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    Academic Journal

    المساهمون: Статья подготовлена в рамках научно-исследовательской работы (№/№ государственных заданий РК 122040400024-7) и международного научного сотрудничества ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой» (Россия) с Казахским Национальный Медицинским Университетом им. С.Д. Асфендиярова (Казахстан).

    المصدر: Modern Rheumatology Journal; Том 18, № 2 (2024); 7–15 ; Современная ревматология; Том 18, № 2 (2024); 7–15 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/1556/1452; Van Beers JJBC, Vanderlocht J, Roozendaal C, Damoiseaux J. Detection of anti-neutrophil cytoplasmic antibodies (ANCA) by indirect immunofluorescence. Methods Mol Biol. 2019:1901:47-62. doi:10.1007/978-14939-8949-2_4.; Csernok EJ, Damoiseaux N, Hellmich RB,et al. Evaluation of automated multi-parametric indirect immunofluorescence assays to detect anti-neutrophil cytoplasmic antibodies (ANCA) in granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA). Autoimmun Rev. 2016 Jul;15(7):736-41. doi:10.1016/j.autrev.2016.03.010. Epub 2016 Mar 9.; Mukhtyar C, Flossmann O, Hellmich B, et al. Outcomes from studies of antineutrophil cytoplasm antibody associated vasculitis: a systematic review by the European League Against Rheumatism systemic vasculitis task force. Ann Rheum Dis. 2008 Jul;67(7):1004-10. doi:10.1136/ard.2007.071936. Epub 2007 Oct 2; Ou CC, Wu YC, Chen JP, et al. Association of atypical anti-neutrophil cytoplasmic antibody with comorbidities and outcome in a hospital-based population. Heliyon. 2024 Jan 6;10(1):e24105. doi:10.1016/j.heliyon.2024.e24105.; Moiseev S, Cohen Tervaert JW, Arimura Y,et al. 2020 international consensus on ANCA testing beyond systemic vasculitis. Autoimmun Rev. 2020 Sep;19(9):102618. doi:10.1016/j.autrev.2020.102618. Epub 2020 Jul 12.; Li W, Chen R, Chen W, et al. Clinicopathological Features and Outcomes of IgA Nephro pathy with Serum Antineutrophil Cytoplasmic Autoantibody Positivity. Am J Nephrol. 2023; 54(9-10):416-424. doi:10.1159/000533982. Epub 2023 Sep 19.; Xiong Q, Lin W, Shen C, et al. Coexistence of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and IgA nephropathy. Immunol Res. 2023 Feb; 71(1):1-14. doi:10.1007/s12026-022-09322-8.; Sato N, Yokoi H, Imamaki H, et al. Renallimited vasculitis with elevated levels of multiple antibodies. CEN Case Rep. 2017 May; 6(1):79-84 doi:10.1007/s13730-017-0248-3. Epub 2017 Mar 3.; Palha V, Sa A, Pimentel T, et al. A rare caseof pulmonary-renal syndrome with triple-seropositive for myeloperoxidase-anti-neutrophil cytoplasm antibody (MPO-ANCA), proteinase 3 (PR3)-ANCA and anti-glomerular basement membrane (GBM) antibodies. J Med Cases. 2021 Oct;12(10):405-410. doi:10.14740/jmc3742.; Olson SW, Arbogast CB, Baker TP, et al.Asymptomatic autoantibodies associate with future anti-glomerular basement membrane disease. J Am Soc Nephrol. 2011 Oct;22(10): 1946-52. doi:10.1681/ASN.2010090928. Epub 2011 Aug 25.; Matsuno S, Itabashi M, Komatsu A, et al.Anti-glomerular basement membrane disease developing 3 years after the development of Sweet syndrome and 1 year after the development of anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report. CEN Case Rep. 2023 Aug;12(3):259-264. doi:10.1007/s13730-022-00758-3.; Fogo AB, Lusco MA, Najafian B, Alpers CE. AJKD Atlas of Renal Pathology: Anti-Glomerular Basement Membrane Antibody-Mediated Glomerulonephritis. Am J Kidney Dis. 2016 Nov;68(5):e29-e30. doi:10.1053/j.ajkd.2016.09.003.; Zhao J, Yang R, Cui Z, et al. Characteristics and outcome of Chinese patients with both antineutrophil cytoplasmic antibody and antiglomerular basement membrane antibodies. Nephron Clin Pract. 2007;107(2):c56-62. doi:10.1159/000107803.; McAdoo SP, Pusey CD. Antiglomerularbasement membrane disease. Semin Respir Crit Care Med. 2018 Aug;39(4):494-503. doi:10.1055/s-0038-1669413.; McAdoo SP, Tanna A, Hruskova Z, et al. Patients double-seropositive for ANCA and anti-GBM antibodies have varied renal survival, frequency of relapse, and outcomes compared to single-seropositive patients. Kidney Int. 2017 Sep;92(3):693-702. doi:10.1016/j.kint.2017.03.014.; Van Daalen EE, Jennette JC, McAdoo SP,et al. Predicting outcome in patients with anti-GBM glomerulonephritis. 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Biomedicines. 2023 Nov 6;11(11): 2978. doi:10.3390/biomedicines11112978.; Rutgers A, Slot M, van Passen P, et al.Coexistence of anti-glomerular basement membrane antibodies and myeloperoxidaseANCAs in crescentic glomerulonephritis. Am. Kidney Dis. 2005 Aug;46(2):253-62. doi:10.1053/j.ajkd.2005.05.003.; Sadeghi-Alavijeh O, Henderson S, Bass P,et al. Crescentic glomerulonephritis with antiGBM antibody but no glomerular deposition. BMC Nephrol. 2018 Sep 12;19(1):228. doi:10.1186/s12882-018-1027-x.; Petri М, Orbai AM, Alarcуn GS, et al. Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus. Arthritis Rheumatol. 2012 Aug;64(8): 2677-86. doi:10.1002/art.34473.; Tervaert JW, Mulder AH, Kallenberg CG. Perinuclear antineutrophil cytoplasmic antibodies (p-ANCA): clinical significance and relation to antibodies against myeloid lysosomal enzymes. 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Autoimmun Rev. 2022 Jun;21(6):103099. doi:10.1016/j.autrev.2022.103099. Epub 2022 Apr 19.; Pillay SS, Nune A, Manzo C, et al. A caseof anti-neutrophil cytoplasmic antibody-associated vasculitis masquerading as Sjögren syndrome. Int J Rheum Dis. 2023 Dec;26(12): 2555-2558. doi:10.1111/1756-185X.14823.; Kaynar K, Güvercin B, Sengör A, Mungan S. A case of Sjögren syndrome and antineutrophil cytoplasmic antibody-associated vasculitis. Reumatismo. 2023 Jul 17;75(2). doi:10.4081/reumatismo.2023.1564; Font J, Ramos-Casals M, Cervera R, et al. Antineutrophil cytoplasmic antibodies in primary Sjögren’s syndrome: prevalence and clinical significance. Br J Rheumatol. 1998 Dec; 37(12):1287-91. doi:10.1093/rheumatology/37.12.1287.; Zhang W, Stone JH. Management of IgG4-related disease. Lancet Rheumatol. 2019 Sep;1(1):e55-e65. doi:10.1016/S26659913(19)30017-7. Epub 2019 Aug 28.; Mbengue M, Goumri N, Niang A. IgG4related kidney disease: pathogenesis, diagnosis, and treatment. 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The uncertain meaning of ANCApositivity in IgG4-related disease. Rheumatology (Oxford). 2021 Aug 2;60(8):3492-3493. doi:10.1093/rheumatology/keab368.; Kuske L, Khalifa А, Wibisono А, et al. MPO-ANCA-positive granulomatosis with polyangiitis and concurrent IgG4-related disease with periaortitis and tubulointerstitial nephritis: A case report of a new overlap syndrome? Int J Rheum Dis. 2023 Sep;26(9):18211825. doi:10.1111/1756-185X.14680; Wu HHL, Wang CCY, Woywodt A, Ponnusamy A. Concurrent presentation of IgG4related tubulointerstitial nephritis and ANCA MPO crescentic glomerulonephritis. Clin Nephrol Case Stud. 2022 Jul 4;10:47-53. doi:10.5414/CNCS110852.eCollection 2022.; Gilani SI, Alexander MP, Nasr SH, et al. Clinicopathologic findings in mass forming ANCA-associated vasculitis. Kidney Int Rep. 2022 Sep 29;7(12):2709-2713. doi:10.1016/j.ekir.2022.09.019.eCollection 2022 Dec.; Ferry JA, Klepeis V, Sohani AR, et al. 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Rheumatology (Oxford). 2000 May; 39(5):481-9. doi:10.1093/rheumatology/39.5.481.; Kida I, Kobayashi S, Takeuchi K, et al.Antineutrophil cytoplasmic antibodies against myeloperoxidase, proteinase 3, elastase, cathepsin G and lactoferrin in Japanese patients with rheumatoid arthritis. Mod Rheumatol. 2011 Feb;21(1):43-50. doi:10.1007/s10165010-0356-9. Epub 2010 Sep 28.; Gуis M, Messias A, Carvalho D et al. MPO-ANCA-associated necrotizing glomerulonephritis in rheumatoid arthritis; a case report and review of literature. J Nephropathol. 2017 Mar;6(2):58-62. doi:10.15171/jnp.2017.10. Epub 2016 Oct 27.; Wu Н, Lu Y, Hu R, et al. Anti-neutrophilcytoplasmic antibody associated vasculitis in patients with rheumatoid arthritis. BMC Nephrol. 2022 Apr 22;23(1):155. doi:10.1186/s12882-022-02788-6.; Nada AK, Torres VE, Ryu JH, et al. Pulmonary fibrosis as an unusual clinical manifestation of a pulmonary-renal vasculitis in elderly patients. Mayo Clin Proc. 1990 Jun; 65(6):847-56. doi:10.1016/s0025-6196(12) 62575-0.; Arimura Y, Minoshima S, Tanaka U, et al.Pulmonary involvement in patients with myeloperoxidase specific-antineutrophil cytoplasmic antibody. Ryumachi Rheum. 1995 Feb; 35(1):46-55.; Pella E, Iatridi F, Sgouropoulou V, et al.Pulmonary involvement in antineutrophil cytoplasmic antibody-associated vasculitides. Int J Rheum Dis. 2024 Jan;27(1):e14933. doi:10.1111/1756-185X.14933.; Yamaguchi K, Yamaguchi A, Ito M, et al. Clinical differences among patients with myeloperoxidase-antineutrophil cytoplasmic antibody-positive interstitial lung disease. Clin Rheumatol. 2023 Feb;42(2):479-488. doi:10.1007/s10067-022-06388-5.; Steward M, Thould H, Myat Noe Khin A, Gibbons MA. Interstitial Lung Disease and Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis: A Review. Immunol Allergy Clin North Am. 2023 May;43(2):379-388. doi:10.1016/j.iac.2023.01.001.; Sebastiani M, Manfredi A, Vacchi C, et al. Epidemiology and management of interstitial lung disease in ANCA-associated vasculitis. Clin Exp Rheumatol. 2020 Mar-Apr;38 Suppl 124(2):221-231.; Matsuda S, Kotani T, Suzuka T, et al. Evaluation of poor prognostic factors of respiratory related death in microscopic polyangiitis complicated by interstitial lung disease. Sci Rep. 2021 Jan 15;11(1):1490. doi:10.1038/s41598-021-81311-7.; Шелыгин ЮА, Ивашкин ВТ, Ачкасов СИи др. Клинические рекомендации. Болезнь Крона (К50), взрослые. Колопроктология. 2023;22(3):10-49.; Drury B, Hardisty G, Gray RD, Ho GT.Neutrophil Extracellular Traps in Inflammatory Bowel Disease: Pathogenic Mechanisms and Clinical Translation. Cell Mol Gastroenterol Hepatol. 2021;12(1):321-333. doi:10.1016/j.jcmgh.2021.03.002. Epub 2021 Mar 6.; Calabresi P, Thayer WR Jr, Spiro HM. Demonstration of circulating antinuclear globulins in ulcerative colitis. J Clin Invest. 1961 Dec; 40(12):2126-33. doi:10.1172/JCI104438.; Prideaux L, De Cruz P, Ng SC, Kamm MA.Serological antibodies in inflammatory bowel disease: A systematic review. Inflamm Bowel Dis. 2012 Jul;18(7):1340-55. doi:10.1002/ibd.21903.; Andalucнa C, Martinez-Prat L, Bentow C,et al. Clinical Validity of Anti-Proteinase 3 Antibodies in Patients with Inflammatory Bowel Disease: A Short Meta-Analysis. Diagnostics (Basel). 2023 Dec 16;13(24):3682. doi:10.3390/diagnostics13243682.; Александрова ЕН, Новиков АА, Лукина ГВ, Парфенов АИ. Клиническое значение антител при воспалительных заболеваниях кишечника. Терапевтический архив. 2021;93(2):228-235.; Pagnoux C, Mahr A, Cohen P, Guillevin L.Presentation and outcome of gastrointestinal involvement in systemic necrotizing vasculitides: analysis of 62 patients with polyarteritis nodosa, microscopic polyangiitis, Wegener granulomatosis, Churg–Strauss syndrome, or rheumatoid arthritis-associated vasculitis. Medicine (Baltimore). 2005 Mar;84(2):115-128. doi:10.1097/01.md.0000158825.87055.0b.; Beretta-Piccoli ВТ, Mieli-Vergani G, Vergani D. Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice. Clin Rev Allergy Immunol. 2022 Oct;63(2):124-137. doi:10.1007/s12016-021-08888-9; De Riva V, Celadin M, Pittoni M, et al. What is behind the presence of antineutrophil cytoplasmatic antibodies in chronic liver disease? Liver Int. 2009 Jul;29(6):865-70. doi:10.1111/j.1478-3231.2009.01989.x.; Hutson TE, Hoffman GS. Temporal concurrence of vasculitis and cancer: a report of 12 cases. Arthritis Care Res. 2000 Dec;13(6): 417-23. doi:10.1002/1529-0131(200012)13:63.0.co;2-t.; Chiao-Chi Ou , Yen-Ching Wu , JunPeng, et al. Chen Association of atypical antineutrophil cytoplasmic antibody with comorbidities and outcome in a hospital-based population. Heliyon. 2024 Jan 6;10(1):e24105. doi:10.1016/j.heliyon.2024.e24105.; Houben E, Bax WA, van Dam B, et al. Diagnosing ANCA-associated vasculitis in ANCA positive patients: A retrospective analysis on the role of clinical symptoms and the ANCA titre. Medicine (Baltimore). 2016 Oct; 95(40):e5096. doi:10.1097/MD.0000000000005096.; Zhang CY, Miao R, Li W, et al. Lung adenocarcinoma and sequential antineutrophil cytoplasmic antibody-associated vasculitis: a case report. J Int Med Res. 2021 Feb;49(2): 300060521993319. doi:10.1177/0300060521993319.; Quack H, Erpenbeck L, Wolff HA, et al.Oxaliplatin-induced leukocytoclastic vasculitis under adjuvant chemotherapy for colorectal cancer: two cases of a rare adverse event. Case Rep Oncol. 2013 Dec 11;6(3):609-15. doi:10.1159/000357166.; Mattiassich G, Egger M, Semlitsch G,Rainer F. Occurrence of relapsing polychondritis with a rising cANCA titre in a cANCApositive systemic and cerebral vasculitis patient. BMJ Case Rep. 2013 Feb 15;2013: bcr2013008717. doi:10.1136/bcr-2013008717.; Iwuji K, Kanu A, Stroever S, et al. Clinicalsignificance of BPI-ANCA in patients with cystic fibrosis: a single center prospective study. Sci Rep. 2023 Oct 24;13(1):18138. doi:10.1038/s41598-023-45273-2.; Alqurashi AS, Aly MH, Mohammed A, et al. Dermatological Lesions of Cholesterol Syndrome and Kaposi Sarcoma Mimic Primary Systemic Vasculitis: Case report study. Sultan Qaboos Univ Med J. 2023 May;23(2): 256-258. doi:10.18295/squmj.2.2022.018.; Konstantinov KN, Ulff-Møller CJ, Tzamaloukas AH. Infections and antineutrophil cytoplasmic antibodies: triggering mechanisms. Autoimmun Rev. 2015 Mar;14(3):201-3. doi:10.1016/j.autrev.2014.10.020.; Banjongjit А, Thammathiwat Т, Townamchai N, Kanjanabuch Т. SARS-CoV-2 infection associated with antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis (ANCA-GN): a systematic review and two case reports. J Nephrol. 2024 Jan; 37(1):53-63. doi:10.1007/s40620-023-01777-8. Epub 2023 Nov 6.; Schaap CM, Krol RM, Remmelts HHF, et al. The effect of nasal Staphylococcus aureus colonization and antibiotic treatment on disease activity in ANCA-associated vasculitis: a retrospective cohort study in the Netherlands. Rheumatol Int. 2023 Mar;43(3):467-475. doi:10.1007/s00296-022-05228-8.; Van Gool IC, Kers J, Bakker JA, et al. Antineutrophil cytoplasmic antibodies in infective endocarditis: a case report and systematic review of the literature. Clin Rheumatol. 2022 Oct;41(10):2949-2960. doi:10.1007/s10067022-06240-w.; Huan G, Yang G, Xiao-Yu Q, et al. Antineutrophil cytoplasmic antibodies in Chinese patients with tuberculosis. Rev Soc Bras Med Trop. 2018 Jul-Aug;51(4):475-478. doi:10.1590/0037-8682-0400-2017.; Culerrier J, Nguyen Y, Karadag O, Bilge SY. Characteristics and outcome of ANCA-associated vasculitides induced by anti-thyroid drugs: a multicenter retrospective case-control study. Rheumatology (Oxford). 2023 Jun 24:kead319. doi:10.1093/rheumatology/kead319; Geetha D, Jefferson JA. ANCA-Associated Vasculitis: Core Curriculum 2020. Am J Kidney Dis. 2020 Jan;75(1):124-137. doi:10.1053/j.ajkd.2019.04.031.; Yaseen K, Nevares A, Tamaki H. A Spotlight on Drug-Induced Vasculitis. Curr Rheumatol Rep. 2022 Nov;24(11):323-336. doi:10.1007/s11926-022-01088-0; Seida I, Seida R, Elsalti A, Mahroum N.Vaccines and Autoimmunity-From Side Effects to ASIA Syndrome. Medicina (Kaunas). 2023 Feb 14;59(2):364. doi:10.3390/medicina59020364; Nune A, Durkowski V, Pillay SS, et al. New-Onset Rheumatic Immune-Mediated Inflammatory Diseases Following SARSCoV-2 Vaccinations until May 2023: A Systematic Review. Vaccines (Basel). 2023 Oct 8; 11(10):1571. doi:10.3390/vaccines11101571; Watad A, Quaresma M, Bragazzi NL, et al. The autoimmune/inflammatory syndrome induced by adjuvants (ASIA)/Shoenfeld’s syndrome: descriptive analysis of 300 patients from the international ASIA syndrome registry. Clin Rheumatol. 2018 Feb;37(2):483-493. doi:10.1007/s10067-017-3748-9.; https://mrj.ima-press.net/mrj/article/view/1556

  2. 2
    Academic Journal

    المساهمون: Статья подготовлена в рамках научно-исследовательской работы (№/№ государственных заданий РК 122040400024-7) и международного сотрудничества ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой» (Россия) и Национального центра кардиологии и терапии им. акад. Мирсаида Миррахимова при Министерстве здравоохранения Кыргызской республики (Кыргызстан).

    المصدر: Modern Rheumatology Journal; Том 18, № 1 (2024); 101-108 ; Современная ревматология; Том 18, № 1 (2024); 101-108 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/1539/1445; Seko Y , Takahashi N, Tada Y, et al. Restricted usage of T-cell receptor VgammaVdelta genes and expression of costimulatory molecules in Takayasu's arteritis. Int J Cardiol. 2000 Aug 31;75 Suppl 1:S77-83; discussion S85-7. doi:10.1016/s0167-5273(00)00194-7.; Ohigashi H, Haraguchi G, Konishi M, et al. Improved prognosis of Takayasu arteritis over the past decade. Circ J. 2012;76(4): 1004-11. doi:10.1253/circj.cj-11-1108. Epub 2012 Feb 2.; Schmidt J, Kermani TA, Bacani AK, et al. Diagnostic features, treatment, and outcomes of Takayasu arteritis in a US Cohort of 126 patients. Mayo Clin Proc. 2013 Aug;88(8): 822-30. doi:10.1016/j.mayocp.2013.04.025. Epub 2013 Jul 10.; Gudbrandsson B, Molberg O, Garen T, Palm O. Prevalence, Incidence, and Disease Characteristics of Takayasu Arteritis by Ethnic Background: Data From a Large, PopulationBased Cohort Resident in Southern Norway. Arthritis Care Res (Hoboken). 2017 Feb;69(2): 278-285. doi:10.1002/acr.22931. Epub 2016 Dec 31.; Watanabe Y, Miyata T, Tanemoto K. Current Clinical Features of New Patients With Takayasu Arteritis Observed From Cross-Country Research in Japan: Age and Sex Specificity. Circulation. 2015 Nov 3;132(18):1701-9. doi:10.1161/CIRCULATIONAHA.114. 012547. Epub 2015 Sep 9.; Firouzi A , Khalilipur E, Khajali Z, et al. The Treatment Dilemma of Arteriopathy in Takayasu Arteritis – A State-of-the-Art Approach. Curr Probl Cardiol. 2023 Jan; 48(1): 101359. doi:10.1016/j.cpcardiol.2022.101359.; Zhang Z, Wang W, Zhou M, et al. Observational Study of Sex Differences in Takayasu Arteritis in China: Implications for Worldwide Regional Differences. Ann Vasc Surg. 2020 Jul:66:309-317. doi:10.1016/j.avsg.2019.12.007. Epub 2019 Dec 18.; Rutter M, Bowley J, Lanyon PC, et al. A Systematic Review and Meta-Analysis of the Incidence Rate of Takayasu Arteritis. Rheumatology (Oxford). 2021; Nov 3;60(11): 4982-4990. doi:10.1093/rheumatology/ keab406.; Isohisa I, Numano F, Maezawa H, Sasazuki T. HLA-Bw52 in Takayasu disease. Tissue Antigens. 1978 Oct;12(4):246-8. doi:10.1111/j.1399-0039.1978.tb01332.x.; Naito S, Arakawa K, Saito S, et al. Takayasu's disease: association with HLA-B5. Tissue Antigens. 1978 Aug;12(2):143-5. doi:10.1111/j.1399-0039.1978.tb01310.x.; Terao C. Revisited HLA and non-HLA genetics of Takayasu arteritis – where are we? J Hum Genet. 2016 Jan;61(1):27-32. doi:10.1038/jhg.2015.87. Epub 2015 Jul 16.; Saruhan-Direskeneli G, Hughes T, Aksu K, et al. Identification of multiple genetic susceptibility loci in Takayasu arteritis. Am J Hum Genet. 2013 Aug 8;93(2):298-305. doi:10.1016/j.ajhg.2013.05.026. Epub 2013 Jul 3.; Renauer PA, Saruhan-Direskeneli G, Coit P, et al. Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study. Arthritis Rheumatol. 2015 May;67(5): 1361-8. doi:10.1002/art.39035.; Renauer P, Sawalha AH. The genetics of Takayasu arteritis. Presse Med. 2017 Jul-Aug; 46(7-8 Pt 2):e179-e187. doi:10.1016/j.lpm.2016.11.031. Epub 2017 Jul 26.; Ortiz-Fernandez L, Saruhan-Direskeneli G, Alibaz-Oner F, et al. Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Am J Hum Genet. 2021 Jan 7;108(1): 84-99. doi:10.1016/j.ajhg.2020.11.014. Epub 2020 Dec 11.; Carmona FD, Coit P, Saruhan-Direskeneli G, et al. Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy. Sci Rep. 2017 Mar 9:7:43953. doi:10.1038/srep43953.; Jin K, Wen Z, Wu B, et al. NOTCH-induced rerouting of endosomal trafficking disables regulatory T cells in vasculitis. J Clin Invest. 2021 Jan 4;131(1):e136042. doi:10.1172/JCI136042.; Daxini A, Cronin K, Sreih AG. Vasculitis associated with immune checkpoint inhibitors-a systematic review. Clin Rheumatol. 2018 Sep;37(9):2579-2584. doi:10.1007/s10067-018-4177-0. Epub 2018 Jun 19.; Pryshchep O, Ma-Krupa W, Younge BR, et al.Vessel-specific Toll-like receptor profiles in human medium and large arteries. Circulation. 2008 Sep 16;118(12):1276-84. doi:10.1161/CIRCULATIONAHA.108.789172. Epub 2008 Sep 2.; Kaiser M, Younge B, Björnsson J, et al. Formation of new vasa vasorum in vasculitis. Production of angiogenic cytokines by multinucleated giant cells. Am J Pathol. 1999 Sep; 155(3):765-74. doi:10.1016/S0002-9440(10) 65175-9.; Desbois AC, Regnier P, Quiniou V, et al. Specific Follicular Helper T Cell Signature in Takayasu Arteritis. Arthritis Rheumatol. 2021 Jul;73(7):1233-1243. doi:10.1002/art.41672. Epub 2021 May 19.; Hoyer BF, Mumtaz IM, Loddenkemper K, et al. Takayasu arteritis is characterised by disturbances of B cell homeostasis and responds to B cell depletion therapy with rituximab. Ann Rheum Dis. 2012 Jan;71(1):75-9. doi:10.1136/ard.2011.153007. Epub 2011 Sep 27.; Grayson PC, Ponte C, Suppiah R, et al. 2022 American College of Rheumatology/ EULAR classification criteria for Takayasu arteritis. Ann Rheum Dis. 2022 Dec;81(12): 1654-1660. doi:10.1136/ard-2022-223482. Epub 2022 Nov 9.; Misra DP, Singh K, Rathore U, et al. Management of Takayasu arteritis. Best Pract Res Clin Rheumatol. 2023 May 26;101826. doi:10.1016/j.berh.2023.101826.; As C, Danda D. Current Diagnosis and Management of Takayasu Arteritis. Int Heart J. 2023;64(4):519-534. doi:10.1536/ihj.23-195.; Quinn KA, Gribbons KB, Carette S, et al. Patterns of clinical presentation in Takayasu’s arteritis. Semin Arthritis Rheum. 2020 Aug; 50(4):576-581. doi:10.1016/j.semarthrit.2020. 04.012. Epub 2020 May 19.; Keenan NG, Mason JC, Maceira A, et al. Integrated cardiac and vascular assessment in takayasu arteritis by cardiovascular magnetic resonance. Arthritis Rheum. 2009 Nov;60(11): 3501-9. doi:10.1002/art.24911.; Койлубаева ГМ, Болотбекова АМ, Бейшенкулов МТ и др. Клинические проявления поражения сердечно-сосудистой системы и предикторы неблагоприятного прогноза артериита Такаясу у кыргызских пациентов. Научно-практическая ревматология. 2023;61(5):576-583.; Hellmich B, Agueda A, Monti S, et al. 2018 update of the EULAR recommendations for the management of large vessel vasculitis. Ann Rheum Dis. 2020 Jan;79(1):19-30. doi:10.1136/annrheumdis-2019-215672. Epub 2019 Jul 3.; Maz M, Chung SA, Abril A, et al. American college of rheumatology/vasculitis foundation guideline for the management of giant cell arteritis and Takayasu Arteritis. Arthritis Rheumatol. 2021 Aug;73(8):1349-65. doi:10.1002/art.41774 31. Hoffman GS, Leavitt RY, Kerr GS, et al. Treatment of glucocorticoid-resistant or relapsing takayasu arteritis with methotrexate. Arthritis Rheum. 1994 Apr;37(4):578-82. doi:10.1002/art.1780370420.; Valsakumar AK, Valappil UC, Jorapur V, et al. Role of immunosuppressive therapy on clinical, immunological, and angiographic outcome in active Takayasu's arteritis. J Rheumatol. 2003 Aug;30(8):1793-8.; Dai D, Wang YY, Jin H, et al. The efficacy of mycophenolate mofetil in treating Takayasu arteritis: a systematic review and meta-analysis. Rheumatol Int. 2017 Jul;37(7):1083-1088. doi:10.1007/s00296-017-3704-7. Epub 2017 Mar 31.; de Souza AWS, de Almeida Agustinelli R, de Cinque Almeida H, et al. Leflunomide in Takayasu arteritis – a long term observational study. Rev Bras Reumatol Engl Ed. 2016 JulAug;56(4):371-5. doi:10.1016/j.rbre.2016.02.003. Epub 2016 Mar 2.; Sun Y, Ma L, Ma L, et al. Cyclophosphamide could be a better choice than methotrexate as induction treatment for patients with more severe Takayasu's arteritis. Rheumatol Int. 2017 Dec;37(12):2019-2026. doi:10.1007/s00296-017-3847-6. Epub 2017 Oct 13.; Misra DP, Rathore U, Patro P, et al. Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis. Clin Rheumatol. 2021 Nov;40(11):4391-4416. doi:10.1007/s10067-021-05743-2. Epub 2021 May 1.; Barra L, Yang G, Pagnoux C. Non-glucocorticoid drugs for the treatment of Takayasu's arteritis: A systematic review and meta-analysis. Autoimmun Rev. 2018 Jul;17(7):683-693. doi:10.1016/j.autrev.2018.01.019. Epub 2018 May 2.; Mertz P, Kleinmann JF, Lambert M, et al. Infliximab is an effective glucocorticoid-sparing treatment for Takayasu arteritis: results of a multicenter open-label prospective study. Autoimmun Rev. 2020 Oct;19(10):102634. doi:10.1016/j.autrev.2020.102634. Epub 2020 Aug 13.; Clifford A, Hoffman GS. Recent advances in the medical management of Takayasu arteritis: an update on use of biologic therapies. Curr Opin Rheumatol. 2014 Jan;26(1):7-15. doi:10.1097/BOR.0000000000000004.; Mekinian A, Comarmond C, Resche-Rigon M, et al. Efficacy of biological-targeted treatments in takayasu arteritis: multicenter, retrospective study of 49 patients. Circulation. 2015 Nov 3;132(18):1693-700. doi:10.1161/CIRCULATIONAHA.114.014321. Epub 2015 Sep 9.; Suematsu R, Tashiro S, Ono N, et al. Successful golimumab therapy in four patients with refractory Takayasu's arteritis. Mod Rheumatol. 2018 Jul;28(4):712-715. doi:10.3109/14397595.2015.1134393. Epub 2016 Mar 21.; Novikov PI, Smitienko IO, Sokolova MV, et al. Certolizumab pegol in the treatment of takayasu arteritis. Rheumatology (Oxford). 2018 Dec 1;57(12):2101-2105. doi:10.1093/rheumatology/key197.; Nishimoto N, Nakahara H, Yoshio-Hoshino N, Mima T. Successful treatment of a patient with Takayasu arteritis using a humanized anti-interleukin-6 receptor antibody. Arthritis Rheum. 2008 Apr;58(4):1197-200. doi:10.1002/art.23373.; Abisror N, Mekinian A, Lavigne C, et al. Tocilizumab in refractory Takayasu arteritis: a case series and updated literature review. Autoimmun Rev. 2013 Oct;12(12):1143-9. doi:10.1016/j.autrev.2013.06.019. Epub 2013 Jun 29.; Canas CA, Canas F, Izquierdo JH, et al. Efficacy and safety of anti-interleukin 6 receptor monoclonal antibody (tocilizumab) in colombian patients with takayasu arteritis. J Clin Rheumatol. 2014 Apr;20(3):125-9. doi:10.1097/RHU.0000000000000098.; Koster MJ, Matteson EL, Warrington KJ. Recent advances in the clinical management of giant cell arteritis and Takayasu arteritis. Curr Opin Rheumatol. 2016 May;28(3):211-7. doi:10.1097/BOR.0000000000000265.; Wang J, Kong X, Ma L, et al. Treatment efficacy and safety of adalimumab versus tocilizumab in patients with active and severe Takayasu arteritis: an open-label study. Rheumatology (Oxford). 2023 Aug 4:kead387. doi:10.1093/rheumatology/kead387. Online ahead of print.; Upendra Rathore U, Thakare DR, Patro P, et al. A systematic review of clinical and preclinical evidences for Janus kinase inhibitors in large vessel vasculitis. Clin Rheumatol. 2022 Jan;41(1):33-44. doi:10.1007/s10067-021-05973-4. Epub 2021 Nov 3; Kong X, Sun Y, Dai X, et al. Treatment efficacy and safety of tofacitinib vs. methotrexate in Takayasu arteritis: a prospective observational study. Ann Rheum Dis. 2022 Jan;81(1): 117-123. doi:10.1136/annrheumdis-2021-220832.; Li J, Li M, Tian X, Zeng X. Tofacitinib in patients with refractory Takayasu's arteritis. Rheumatology (Oxford). 2020 Nov 1;59(11): e95-e98. doi:10.1093/rheumatology/keaa281.; Sato S, Matsumoto H, Temmoku J, et al. A case of Takayasu arteritis complicated by refractory ulcerative colitis successfully treated with tofacitinib. Rheumatology (Oxford). 2020 Jul 1;59(7):1773-1775. doi:10.1093/rheumatology/kez580.; Palermo A, Marvisi C, Casali M, et al. Tofacitinib for the treatment of refractory Takayasu's arteritis: description of 2 cases. Clin Exp Rheumatol. 2020 Mar-Apr;38 Suppl 124(2):234-235. Epub 2020 Jan 9.; Regnier P, Le Joncour A, MaciejewskiDuval A, et al. Targeting JAK/STAT pathway in Takayasu's arteritis. Ann Rheum Dis. 2020 Jul;79(7):951-959. doi:10.1136/annrheumdis-2019-216900. Epub 2020 Mar 25.; Watanabe R. JAK inhibitors as promising agents for refractory Takayasu arteritis. Ann Rheum Dis. 2022 Apr;81(4):e67. doi:10.1136/ annrheumdis-2020-217577; Inder SJ, Bobryshev YV, Cherian SM, et al. Immunophenotypic analysis of the aortic wall in Takayasu's arteritis: involvement of lymphocytes, dendritic cells and granulocytes in immuno-inflammatory reactions. Cardiovasc Surg. 2000 Mar;8(2):141-8. doi:10.1016/s0967-2109(99)00100-3.; Galarza C, Valencia D, Tobуn GJ, et al. Should rituximab be considered as the firstchoice treatment for severe autoimmune rheumatic diseases? Clin Rev Allergy Immunol. 2008 Feb;34(1):124-8. doi:10.1007/s12016-007-8028-z.; Pazzola G, Muratore F, Pipitone N, et al. Rituximab therapy for Takayasu arteritis: a seven patients experience and a review of the literature. Rheumatology (Oxford). 2018 Jul 1; 57(7):1151-55. doi:10.1093/rheumatology/kex249.; Mekinian A, Noe L, Salvarani C, et al. Effectiveness and safety of rituximab in Takayasu arteritis: data from a multicenter retrospective study. Joint Bone Spine. 2023 Oct 31; 91(2):105658. doi:10.1016/j.jbspin.2023.105658.; Nakagomi D, Kronbichler A, Witte T, et al. Comment on: Rituximab therapy for Takayasu arteritis: a seven patients experience and a review of the literature. Rheumatology (Oxford). 2018 Jul 1;57(7):1309-1310. doi:10.1093/rheumatology/kex493.; Caltran E, Di Colo G, Ghigliotti G, et al. Two Takayasu arteritis patients successfully treated with rituximab. Clin Rheumatol. 2014 Aug;33(8):1183-4. doi:10.1007/s10067-014-2506-5. Epub 2014 Jan 31.; Mutoh T, Ishii T, Shirai T, et al. Refractory Takayasu arteritis successfully treated with rituximab: case-based review. Rheumatol Int. 2019 Nov;39(11):1989-1994. doi:10.1007/s00296-019-04390-w. Epub 2019 Aug 6.; Blache U, Tretbar S, Koehl U, et al. CAR T cells for treating autoimmune diseases. RMD Open. 2023 Nov 23;9(4):e002907. doi:10.1136/rmdopen-2022-002907.; Kwon OC, Oh JS, Park MC, et al. Statins reduce relapse rate in Takayasu arteritis. Int J Cardiol. 2019 Jul 15:287:111-115. doi:10.1016/j.ijcard.2019.02.046. Epub 2019 Feb 20.; Laurent C, Prieto-Gonzalez S, Belnou P, et al. Prevalence of cardiovascular risk factors, the use of statins and of aspirin in Takayasu Arteritis. Sci Rep. 2021 Jul 13;11(1):14404. doi:10.1038/s41598-021-93416-0.; Shi G, Hua M, Xu Q, Ren T. Resveratrol improves treatment outcome and laboratory parameters in patients with Takayasu arteritis: A randomized double-blind and placebocontrolled trial. Immunobiology. 2017 Feb; 222(2):164-168. doi:10.1016/j.imbio.2016.10.008. Epub 2016 Oct 14.; Shao N, Jia H, Li Y, Li J. Curcumin im proves treatment out come of Takayasu arteritis patients by reducing TNF-α: a randomized placebo-controlled double-blind clinical trial. Immunol Res. 2017 Aug;65(4):969-974. doi:10.1007/s12026-017-8917-z.; Dejaco C, Ramiro S, Duftner C, et al. EULAR recommendations for the use of imaging in large vessel vasculitis in clinical practice. Ann Rheum Dis. 2018 May;77(5):636-643. doi:10.1136/annrheumdis-2017-212649. Epub 2018 Jan 22.; Padiyar S, Manikuppam P, Kabeerdoss J, et al. Update on pregnancy in Takayasu arteritis-A narrative review. Int J Rheum Dis. 2021 Jun;24(6):758-765. doi:10.1111/1756-185X.14109. Epub 2021 Apr 18.; Chen ST, Luo CB, Guo WY, Chang FC. Endovascular management of symptomatic stenosis of supra-aortic arteries in patients with Takayasu arteritis. J Chin Med Assoc. 2021 Mar 1;84(3):303-308. doi:10.1097/JCMA.0000000000000479.; Han HS, Yoon KW, Heo SH, et al. Aortocarotid bypass in patients with Takayasu’s arteritis. Ann Surg Treat Res. 2017 Sep;93(3): 143-151. doi:10.4174/astr.2017.93.3.143. Epub 2017 Aug 30.; Xiao Y, Zhou J, Wei X, et al. Outcomes of different treatments on Takayasu’s arteritis. J Thorac Dis. 2016 Sep;8(9):2495-2503. doi:10.21037/jtd.2016.08.12.; Chen ZG, Chen YX, Diao YP, et al. Simultaneous Multi-Supra-Aortic Artery Bypass Successfully Implemented in 17 Patients with Type I Takayasu Arteritis. Eur J Vasc Endovasc Surg. 2018 Dec;56(6):903-909. doi:10.1016/j.ejvs.2018.08.044. Epub 2018 Oct 11.; Fu Y, Chen Y. Operative experience on descending aorta with Takayasu Arteritis: a review. Front Cardiovasc Med. 2023 Jun 21:10:1181285. doi:10.3389/fcvm.2023. 1181285. eCollection 2023.; https://mrj.ima-press.net/mrj/article/view/1539

  3. 3
    Academic Journal

    المساهمون: The article was prepared within the framework of a research work, №/№ of state assignments РК 122040400024-7. The investigation has not been sponsored, Статья подготовлена в рамках научно-исследовательской работы, № государственного задания РК 122040400024-7. Исследование не имело спонсорской поддержки

    المصدر: Modern Rheumatology Journal; Том 18, № 3 (2024); 78-84 ; Современная ревматология; Том 18, № 3 (2024); 78-84 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

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Pediatrics.1952;(9):722-28.; Imbach P, Barandun S, Baumgartner C, et al.High-dose intravenous gamma globulin therapy of refractory, in particular idiopathic thrombocytopenia in childhood. Helv Paediatr Acta. 1981 Feb;36(1):81-6.; Saeedian M, Randhawa I. Immunoglobulin replacement therapy: a twenty-year review and current update. Int Arch Allergy Immunol. 2014;164(2):151-66. doi:10.1159/000363445. Epub 2014 Jul 10.; Wood JG, Heywood AE, Dennington PM, et al. Trends in intravenous immunoglobulin use in New South Wales, Australia. Intern Med J. 2024 Jan;54(1):149-156. doi:10.1111/imj.16175.; Velikova T, Sekulovski M, Bogdanova S, et al. Intravenous immunoglobulins as immunomodulators in autoimmune diseases and reproductive medicine. Antibodies (Basel). 2023 Mar 2;12(1):20. doi:10.3390/antib12010020.; National Blood Authority. National report on the issue and use of immunoglobulin (IVIg). Annual report 2015–16. Canberra: Common-wealth of Australia; 2017. https://www.blood.gov.au/data-analysis-reporting.; Tavee J, Brannagan TH 3 rd , Lenihan MW, et al. Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee. Muscle Nerve. 2023 Oct; 68(4):356-74. doi:10.1002/mus.27922.; Danieli MG, Antonelli E, Auria SS, et al. Low-dose intravenous immunoglobulin (IVIg) in different immune-mediated conditions. Autoimmun Rev. 2023 Nov; 22(11):103451. doi:10.1016/j.autrev.2023.103451.; Hadaschik E, Eming R, French LE, et al. European Guidelines (S1) on the use of high-dose intravenous immunoglobulin in dermatology. Hautarzt. 2020 Jul;71(7):542-52. doi:10.1007/s00105-020-04610-6.; Середавкина НВ, Решетняк ТМ, Насонов ЕЛ. Место внутривенного иммуноглобулина при ревматических заболеваниях. Современная ревматология. 2015;9(4):59-67. doi:10.14412/1996-7012-2015-4-59-67.; Gelfand EW. Intravenous immune globulin in autoimmune and inflammatory diseases. N Engl J Med. 2012 Nov 22;367(21):2015-25. doi:10.1056/NEJMra1009433.; Лазанович ВА, Просекова ЕВ. Внутривенные иммуноглобулины: механизмы терапевтических эффектов. Медицинская иммунология. 2014;16(4):311-22.; Shoenfeld Y, Gershwin ME. Intravenous immunoglobulin. Clinic Rev Allerg Immunol. 2005;29:165-66. doi:10.1385/CRIAI:29:3:165.; Bayry J,Fournier EM, Maddur MS, et al. Intravenous immunoglobulin induces proliferation and immunoglobulin synthesis from B cells of patients with common variable immunodeficiency: A mechanism underlying the beneficial effect of IVIg in primary immunodeficiencies. J Autoimmun. 2011 Feb;36(1): 9-15. doi:10.1016/j.jaut.2010.09.006. Epub 2010 Dec 9.; Maddur MS, Kaveri SV, Bayry J. Comparison of different IVIg preparations on IL-17 production by human Th17 cells. Autoimmun Rev. 2011 Oct;10(12):809-10. doi:10.1016/j.autrev.2011.02.007. Epub 2011 Mar 2.; Blank M, Bashi T, Shoenfeld Y. Idiotype-specific intravenous immunoglobulin (IVIG) for therapy of autoimmune diseases. Methods Mol Biol. 2014:1060:353-61. doi:10.1007/978-1-62703-586-6_18.; Hulett MD, Hogarth PM. Molecular Basis of Fc Receptor Function. Adv Immunol. 1994; 57:1-127. doi:10.1016/s0065-2776(08)60671-9.; Spahn JD, Leung DY, Chan MT, et al. Mechanisms of glucocorticoid reduction in asthmatic subjects treated with intravenous immunoglobulin. J Allergy Clin Immunol. 1999 Mar;103(3 Pt 1):421-6. doi:10.1016/s0091-6749(99)70466-5.; Zandman-Goddard G, Krauthammer A, Levy Y, et al. Long-term therapy with intravenous immunoglobulin is beneficial in patients with autoimmune diseases. Clin Rev Allergy Immunol. 2012 Apr;42(2):247-55. doi:10.1007/s12016-011-8278-7.; Dalakas MC. Update on intravenous immunoglobulin in neurology: modulating neuro-autoimmunity, evolving factors on efficacy and dosing and challenges on stopping chronic IVIg therapy. Neurotherapeutics. 2021 Oct;18(4):2397-2418. doi:10.1007/s13311-021-01108-4. Epub 2021 Nov 11.; Benavides-Villanueva F, Loricera J, Calvo-Rio V, et al, Intravenous immunoglobulin therapy in antineutrophil cytoplasmic antibody-associated vasculitis. Eur J Intern Med. 2023 Nov;117:78-84. doi:10.1016/j.ejim.2023.06.021.; Yates M, Watts AR, Bajema IM, et al. EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis. Ann Rheum Dis. 2016 Sep;75(9):1583-94. doi:10.1136/annrheumdis-2016-209133. Epub 2016 Jun 23.; Katz U, Achiron A, Sherer Y, et al. Safety of intravenous immunoglobulin (IVIG) therapy. Autoimmun Rev. 2007 Mar;6(4):257-9. doi:10.1016/j.autrev.2006.08.011. Epub 2006 Aug 28.; Aggarwal R, Schessl J, Charles-Schoeman C, et al. Safety and tolerability of intravenous immunoglobulin in patients with active dermatomyositis: results from the randomised, placebo-controlled ProDERM study. Arthritis Res Ther. 2024 Jan 17;26(1):27. doi:10.1186/s13075-023-03232-2.; Zandman-Goddard G, Levy Y, Shoenfeld Y. Intravenous immunoglobulin therapy and systemic lupus erythematosus. Clin Rev Allergy Immunol. 2005 Dec;29(3):219-28. doi:10.1385/CRIAI:29:3:219.; Toubi E, Kessel A, Shoenfeld Y. High-dose intravenous immunoglobulins: an option in the treatment of systemic lupus erythematosus. Hum Immunol. 2005 Apr;66(4):395-402. doi:10.1016/j.humimm.2005.01.022.; Sherer Y, Kuechler S, Jose Scali J, et al. Low dose intravenous immunoglobulin in systemic lupus erythematosus: analysis of 62 cases. Isr Med Assoc J. 2008 Jan;10(1):55-7.; Binello N, Cancelli C, Passalacqua S, et al. Use of intravenous immunoglobulin therapy at unconventional doses in refractory fulminant systemic lupus erythematosus. Eur J Case Rep Intern Med. 2018 Sep 27;5(9):000934. doi:10.12890/2018_000934. eCollection 2018.; Schroeder J, Zeuner AR, Euler HH, Lцffler H. High dose intravenous immunoglobulins in systemic lupus erythematosus: Clinical and serological results of a pilot study. J Rheumatol. 1996 Jan;23(1):71-5.; Levy Y, Sherer Y, Ahmed A, et al. A study of 20 SLE patients with intravenous immunoglobulin clinical and serologic response. Lupus. 1999;8(9):705-12. doi:10.1191/096120399678841007.; Tenti S, Cheleschi S, Guidelli GM, et al. Intravenous immunoglobulins and antiphospholipid syndrome: How, when and why? A review of the literature. Autoimmun Rev. 2016 Mar;15(3):226-35. doi:10.1016/j.autrev.2015.11.009. Epub 2015 Dec 1.; Sciascia S, Giachino O, Roccatello D. Prevention of thrombosis relapse in anti-phospholipid syndrome patients refractory to conventional therapy using intravenous immunoglobulin. Clin Exp Rheumatol. 2012 May-Jun;30(3):409-13. Epub 2012 Jun 26.; Ruiz-Irastorza G, Espinosa G, Frutos M, et al. Diagnosis and treatment of lupus nephritis: Consensus document from the systemic autoimmune disease group (GEAS) of the Spanish Society of Internal Medicine (SEMI) and the Spanish Society of Nephrology (S.E.N.). Nefrologia. 2012:32 Suppl 1:1-35. doi:10.3265/Nefrologia.pre2011.Dec.11298.; Caccavo D, Vaccaro F, Ferri GM, et al. Antiidiotypes against antiphospholipid anti-bodies are present in normal polyspecific immunoglobulins for therapeutic use. J Autoimmun. 1994 Aug;7(4):537-48. doi:10.1006/jaut.1994.1039.; Horn HC, Grau K, Junker P. IVIG treatment for progressive stroke in the primary antiphospholipid antibody syndrome. Lupus. 2004;13(6):478-80. doi:10.1191/0961203303lu1035cr.; Mulhearn B, Bruce IN. Indications for IVIG in rheumatic diseases. Rheumatology (Oxford). 2015 Mar;54(3):383-91. doi:10.1093/rheumatology/keu429. Epub 2014 Nov 17.; Bitsadze V, Yakubova F, Khizroeva J, et al. Catastrophic Antiphospholipid Syndrome. Int J Mol Sci. 2024 Jan 4; 25(1):668. doi:10.3390/ijms25010668.; Marie I, Menard JF, Hatron PY, et al. Intravenous immunoglobulins for steroid-refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients. Arthritis Care Res (Hoboken). 2010 Dec;62(12):1748-55. doi:10.1002/acr.20325.; Suzuki Y, Hayakawa H, Miwa S, et al. Intravenous immunoglobulin therapy for refractory interstitial lung disease associated with polymyositis/dermatomyositis. Lung. 2009 May-Jun;187(3):201-6. doi:10.1007/s00408-009-9146-6. Epub 2009 Apr 22.; Cherin P, Pelletier S, Teixeira A, et al. Results and long-term follow-up of intravenous immunoglobulin infusions in chronic, refractory polymyositis: An open study with thirty-five adult patients. Arthritis Rheum. 2002 Feb;46(2):467-74. doi:10.1002/art.10053.; Speca S, Farhat MM, Jendoubi M, et al. Intravenous immunoglobulins improve skin fibrosis in experimental models of systemic sclerosis. Sci Rep. 2023 Sep 12;13(1):15102. doi:10.1038/s41598-023-42464-9.; Tandaipan J, Guillen-Del-Castillo A, Simeуn-Aznar CP, et al. Immunoglobulins in systemic sclerosis management. A large multi-center experience. Autoimmun Rev. 2023 Nov; 22(11):103441. doi:10.1016/j.autrev.2023.103441.; Matsuda KM, Yoshizaki A, Kuzumi A, et al. Rapid improvement of systemic sclerosis-associated intestinal pseudo-obstruction with intravenous immunoglobulin administration. Rheumatology (Oxford). 2023 Sep 1; 62(9):3139-45. doi:10.1093/rheumatology/kead093.; Blank M, Levy Y, Amital H, et al. The role of intravenous immunoglobulin therapy in mediating skin fibrosis in high skin mice. Arthritis Rheum. 2002 Jun;46(6):1689-90. doi:10.1002/art.10363.; Richter C, Schnabel A, Csernok E, et al. Treatment of anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis with high-dose intravenous immunoglobulin. Clin Exp Immunol. 1995 Jul;101(1):2-7. doi:10.1111/j.1365-2249.1995.tb02268.x.; Aries PM, Hellmich B, Gross WL. Intravenous immunoglobulin therapy in vasculitis. Clin Rev Allergy Immunol. 2005 Dec;29(3): 237-45. doi:10.1385/CRIAI:29:3:237.; Kivity S, Katz U, Daniel N, et al. Evidence for the use of intravenous immunoglobulins – a review of the literature. Clin Rev Allergy Immunol. 2010 Apr;38(2-3):201-69. doi:10.1007/s12016-009-8155-9.; Chung SA, Langford CA, Maz M, et al. 2021 american college of rheumatology/vasculitis foundation guideline for the management of antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Care Res (Hoboken). 2021 Aug;73(8):1088-1105. doi:10.1002/acr.24634. Epub 2021 Jul 8.; Hellmich В, Sanchez-Alamo В, Schirmer JH, et al. EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update. Ann Rheum Dis. 2024 Jan 2; 83(1):30-47. doi:10.1136/ard-2022-223764.; Jayne D, Chapel H, Adu D, et al. 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Efficacy and Safety of Intravenous Immunoglobulin Treatment in Refractory Behcet's Disease with Different Organ Involvement: A Case Series. Isr Med Assoc J. 2016 Mar-Apr;18 (3-4):238-42.; Seeliger T, Prenzler NK, Gingele S, et al. Neuro-Sjцgren: Peripheral Neuropathy With Limb Weakness in Sjцgren’s Syndrome. Front Immunol. 2019 Jul 11:10:1600. doi:10.3389/fimmu.2019.01600. eCollection 2019.; Mehmood M, Jog A, Niazi M, et al. Atypical 's syndrome initially presenting as lymphocytic interstitial pneumonitis followed by immune thrombocytopenia. Case Rep Rheumatol. 2021 Mar 15;2021:6681590. doi:10.1155/2021/6681590.; Noh G, Han CW. Intravenous Immune Globulin (IVIG) Therapy After Unsuccessful Treatment with Corticosteroid and Cyclosporine A in Pfeifer-Weber-Christian Disease: A Case Report. Am J Case Rep. 2021 Jan 4; 22:e929519. doi:10.12659/AJCR.929519; Shen X, Wang F. The additional treatment value of immunoglobulin for the treatment of rheumatoid arthritis complicated with interstitial lung disease: A propensity score-matched pilot study. Int J Rheum Dis. 2023 Sep; 26(9):1745-1750. doi:10.1111/1756-185X.14808.; Katz-Agranov N, Khattri S, Zandman-Goddard G. The role of intravenous immunoglobulins in the treatment of rheumatoid arthritis. Autoimmun Rev. 2015 Aug; 14(8):651-8. doi:10.1016/j.autrev.2015.04.003. Epub 2015 Apr 12.; Muscat C, Bertotto A, Ercolani R, et al. Long term treatment of rheumatoid arthritis with high doses of intravenous immunoglobulins: effects on disease activity and serum cytokines. Ann Rheum Dis. 1995 May;54(5): 382-5. doi:10.1136/ard.54.5.382.; Kanik KS, Yarboro CH, Naparstek Y, et al. Failure of low-dose intravenous immunoglobulin therapy to suppress disease activity in patients with treatment-refractory rheumatoid arthritis. Arthritis Rheum. 1996 Jun;39(6): 1027-9. doi:10.1002/art.1780390621.; Maksymowych WP, Avina-Zubieta A, Luong M, Russell AS. High dose intravenous immunoglobulin (IVIG) in severe refractory rheumatoid arthritis: no evidence for efficacy. Clin Exp Rheumatol. 1996 Nov-Dec;14(6): 657-60.; Silverman ED, Cawkwell GD, Lovell DJ, et al. Intravenous immunoglobulin in the treatment of systemic juvenile rheumatoid arthritis: a randomized placebo controlled trial. Pediatric Rheumatology Collaborative Study Group. J Rheumatol. 1994 Dec;21(12):2353-8.; https://mrj.ima-press.net/mrj/article/view/1592

  4. 4
    Academic Journal

    المصدر: Rheumatology Science and Practice; Vol 61, No 5 (2023); 576-583 ; Научно-практическая ревматология; Vol 61, No 5 (2023); 576-583 ; 1995-4492 ; 1995-4484

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  5. 5
    Academic Journal

    المساهمون: The article was prepared as a part of the research work (№/№ of government tasks PK 122040400024-7) and international cooperation of V.A. Nasonova Research Institute of Rheumatology (Russia) and the National Center of Cardiology and Therapy named after academician Mirsaid Mirrakhimov at the Ministry of Health of the Kyrgyz Republic (Kyrgyz Republic)., Статья подготовлена в рамках научно-исследовательской работы (№/№ государственных заданий РК 122040400024-7) и международного сотрудничества ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой» (Россия) и Национального центра кардиологии и терапии им. академика Мирсаида Миррахимова при Министерстве здравоохранения Кыргызской республики (Кыргызстан).

    المصدر: Modern Rheumatology Journal; Том 17, № 6 (2023); 122-127 ; Современная ревматология; Том 17, № 6 (2023); 122-127 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

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    Academic Journal

    المساهمون: The article has been conducted within scientific topic № 1021051402790-6 as a part of the government task., Статья подготовлена в рамках научно-исследовательской работы, № государственных заданий 1021051402790-6.

    المصدر: Modern Rheumatology Journal; Том 17, № 4 (2023); 42-49 ; Современная ревматология; Том 17, № 4 (2023); 42-49 ; 2310-158X ; 1996-7012

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    المصدر: Modern Rheumatology Journal; Том 17, № 3 (2023); 37-44 ; Современная ревматология; Том 17, № 3 (2023); 37-44 ; 2310-158X ; 1996-7012

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Inflammatory mechanisms linking obesity and metabolic disease. J Clin Invest. 2017 Jan 3;127(1):1-4. doi:10.1172/JCI92035. Epub 2017 Jan 3.; Daskalogiannaki M, Voloudaki A, Prassopoulos P, et al. CT evaluation of mesenteric panniculitis: prevalence and associated diseases. AJR Am J Roentgenol. 2000 Feb;174(2): 427-31. doi:10.2214/ajr.174.2.1740427.; Patel N, Saleeb S, Teplick S. General case of the day. Mesenteric panniculitis with extensive inflammatory involvement of the peritoneum and intraperitoneal structures. Radiographics. 1999 Jul-Aug;19(4):1083-5. doi:10.1148/radiographics.19.4.g99jl221083.; Kakimoto K, Inoue T, Toshina K, et al. Multiple mesenteric panniculitis as a complication of Sjцgren's Syndrome leading to ileus. Intern Med. 2016;55(2):131-4. doi:10.2169/internalmedicine.55.5407. Epub 2016 Jan 15.; Nomura S, Shimojima Y, Yoshizawa E, et al. Mesenteric panniculitis in systemic lupus erythematosus showing characteristic computed tomography findings. 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Intern Med. 2020 Feb 15;59(4): 513-8. doi:10.2169/internalmedicine.3221-19. Epub 2019 Nov 8.; Emory TS, Monihan JM, Carr NJ, Sobin LH. Sclerosing mesenteritis, mesenteric panniculitis and mesenteric lipodystrophy: a single entity? Am J Surg Pathol. 1997 Apr; 21(4):392-8. doi:10.1097/00000478-199704000-00004.; Eze VN, Halligan S. Mesenteric panniculitis: a clinical conundrum. Br J Radiol. 2023 Feb; 96(1142):20211369. doi:10.1259/bjr.20211369.; Suarez Acosta С, Romero Fernandez Е. Mesenteric panniculitis: A controversial entity. Many unanswered questions. Eur J Intern Med. 2015 Dec;26(10):e67-8. doi:10.1016/j.ejim.2015.09.004.; Alsuhaimi М, Alshowaiey RA, Alsumaihi AS, Aldhafeeri SM. Mesenteric panniculitis various presentations and management: A single institute ten years, experience. Ann Med Surg (Lond). 2022 Aug;80:104203.doi:10.1016/j.amsu.2022.104203; Oztan MO, Ozdemir T, Uncel M, et al. Isolated omental panniculitis in a child with abdominal pain: case report. Arch Argent Pediatr. 2016 Dec 1;114 (6):425. doi:10.5546/aap.2016.eng.e425.; Gögebakan Ö, Osterhoff MA, Albrecht T. Mesenteric panniculitis (MP): A frequent coincidental CT finding of debatable clinical significance. Rofo. 2018 Nov;190(11):1044-52. doi:10.1055/a-0633-3558. Epub 2018 Sep 6.; Badet N, Sailley N, Briquez C, et al. Mesenteric panniculitis: still an ambiguous condition. Diagn Interv Imagin. 2015 Mar;96(3): 251-7. doi:10.1016/j.diii.2014.12.002. Epub 2015 Feb 18.; Delgado Plasencia L, Rodrнguez Ballester L, Lуpez-Tomassetti Fernandez EM, et al. Mesenteric panniculitis: experience in our center. Rev Esp Enferm Dig. 2007 May;99(5): 291-7. doi:10.4321/s1130-01082007000500010.; https://mrj.ima-press.net/mrj/article/view/1429

  8. 8
    Academic Journal

    المساهمون: The article was prepared as part of the research work №/№ of state assignments 1021051402790-6., Статья подготовлена в рамках научно-исследовательской работы №/№ государственных заданий 1021051402790-6.

    المصدر: Modern Rheumatology Journal; Том 17, № 1 (2023); 7-15 ; Современная ревматология; Том 17, № 1 (2023); 7-15 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

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Ann Rheum Dis. 2022 Mar; 81(3):309-14. doi:10.1136/annrheumdis-2021-221794. Epub 2022 Feb 2.; Iudici M, Pagnoux C, Courvoisier DS, et al; French Vasculitis Study Group. Localized versus systemic granulomatosis with polyangiitis: data from the French Vasculitis Study Group Registry. Rheumatology (Oxford). 2022 May 30;61(6):2464-71. doi:10.1093/rheumatology/keab719.; Comarmond C, Cacoub P. Granulomatosis with polyangiitis (Wegener): clinical aspects and treatment. Autoimmun Rev. 2014 Nov;13(11):1121-5. doi:10.1016/j.autrev.2014.08.017. Epub 2014 Aug 20.; Pagnoux C, Stubbe M, Lifermann F, et al. Wegener's granulomatosis strictly and persistently localized to one organ is rare: assessment of 16 patients from the French Vasculitis Study Group database. J Rheumatol. 2011 Mar;38(3):475-8. doi:10.3899/jrheum.100518. Epub 2010 Dec 1.; Holle JU, Gross WL, Holl-Ulrich K, et al. Prospective long-term follow-up of patients with localised Wegener's granulomatosis: does it occur as persistent disease stage? Ann Rheum Dis. 2010 Nov;69(11):1934-9. doi:10.1136/ard.2010.130203. Epub 2010 May 28.; Stone JH. Limited versus severe Wegener’s granulomatosis: baseline data on patients in the Wegener’s granulomatosis etanercept trial. Arthritis Rheum. 2003 Aug;48(8):2299-309. doi:10.1002/art.11075.; Hellmich B, Flossmann O, Gross WL, et al. EULAR recommendations for conducting clinical studies and/or clinical trials in systemic vasculitis: focus on anti-neutrophil cytoplasm antibody-associated vasculitis. Ann Rheum Dis. 2007 May;66(5):605-17. doi:10.1136/ard.2006.062711. Epub 2006 Dec 14.; Куприянова ИН, Орлова ОЛ, Флягина ВИ. Рецидив гранулематоза с полиангиитом после отмены иммуносупрессивной терапии, осложненный стойкой утратой зрения. Русский медицинский журнал. 2018;4(I):35-40.; Anderson G, Coles ET, Crane M, et al. Wegener’s granuloma. A series of 265 British cases seen between 1975 and 1985. A report by a sub-committee of the British Thoracic Society Research Committee. Q J Med. 1992 Jun;83(302):427-38.; Reinhold-Keller E, Beuge N, Latza U, et al. An interdisciplinary approach to the care of patients with Wegener’s granulomatosis: long-term outcome in 155 patients. Arthritis Rheum. 2000 May;43(5):1021-32. doi:10.1002/1529-0131(200005)43:53.0.CO;2-J.; Puechal X, Iudici M, Pagnoux C, et al. French Vasculitis Study Group. Comparative study of granulomatosis with polyangiitis subsets according to ANCA status: data from the French Vasculitis Study Group Registry. RMD Open. 2022 Mar;8(1):e002160. doi:10.1136/rmdopen-2021-002160.; Witko-Sarsat V, Daniel S, Noёl L, Mouthon L. Neutrophils and B lymphocytes in ANCA associated vasculitis. APMIS Suppl. 2009 Jun;(127):27-31. doi:10.1111/j.1600-0463.2009.02473.x.; Preston G, Yang J, Xiao H, Falk R. Understanding the pathogenesis of ANCA: Where are we today? Cleve Clin J Med. 2002; 69 Suppl 2:SII51-4. doi:10.3949/ccjm.69.suppl_2.sii51.; Nakazawa D, Masuda S, Tomaru U, Ishizu A. Pathogenesis and therapeutic interventions for ANCA-associated vasculitis. Nat Rev Rheumatol. 2019 Feb;15(2):91-101. doi:10.1038/s41584-018-0145-y.; Csernok E, Gross WL. Current understanding of the pathogenesis of granulomatosis with polyangiitis (Wegener’s). Expert Rev Clin Immunol. 2013 Jul;9(7):641-8. doi:10.1586/1744666X.2013.811052.; Hua F, Wilde B, Dolff S, Witzke O. T-lymphocytes and disease mechanisms in Wegener's granulomatosis. Kidney Blood Press Res 2009; 32: 389–98.; Lamprecht P., Holle J., Gross W. Update on clinical, pathophysiological and therapeutic aspects in ANCA associated vasculitides. Curr Drug Discov Technol. 2009 Dec;6(4): 241-51. doi:10.2174/157016309789868994.; Лопатина ИА, Моисеев СВ, Новиков ПИ и др. Цитокиновый профиль у пациентов с гранулематозом с полиангиитом. Клиническая фармакология и терапия. 2017;(2):6-11.; Lutalo PM, D'Cruz DP. Diagnosis and classification of granulomatosis with polyangiitis (aka Wegener's granulomatosis). J Autoimmun. 2014 Feb-Mar;48-49:94-8. doi:10.1016/j.jaut.2014.01.028. Epub 2014 Jan 29.; Holl-Ulrich K, Reinhold-Keller E, Müller A, Feller A. Pathology of vasculitis: differential diagnosis and selected disorders. Verh Dtsch Ges Pathol. 2002;86:83-90.; Devaney KO, Travis WD, Hoffman G, et al. Interpretation of head and neck biopsies in Wegener’s granulomatosis. A pathologic study of 126 biopsies in 70 patients. Am J Surg Pathol. 1990 Jun;14(6):555-64. doi:10.1097/00000478-199006000-00006.; Maguchi S, Fukuda S, Takizawa M. Histological findings in biopsies from patients with cytoplasmic-antineutrophil cytoplasmic antibody (cANCA)-positive Wegener's granulomatosis. Auris Nasus Larynx. 2001 May;28 Suppl:S53-8. doi:10.1016/s0385-8146(01)00072-4.; Tan LT, Davagnanam I, Isa H, et al. Clinical and imaging features predictive of orbital granulomatosis with polyangiitis and the risk of systemic involvement. Ophthalmology. 2014 Jun;121(6):1304-9. doi:10.1016/j.ophtha.2013.12.003. Epub 2014 Feb 20.; Ismailova DS, Abramova JV, Novikov PI, Grusha YO. Clinical features of different orbital manifestations of granulomatosis with polyangiitis. Graefes Arch Clin Exp Ophthalmol. 2018 Sep;256(9):1751-6. doi:10.1007/s00417-018-4014-9. Epub 2018 May 30.; Васильев ВИ, Сокол ЕВ, Седышев СХ и др. Дифференциальная диагностика ревматических и онко-гематологических заболеваний, поражающих полость и придаточные пазухи носа. Терапевтический архив. 2014;86(5):62-72.; Rodrigo JP, Suarez C, Rinaldo A, et al. Idiopathic midline destructive disease: fact or fiction. Oral Oncol. 2005 Apr;41(4):340-8. doi:10.1016/j.oraloncology.2004.10.007.; Parker NP, Pearlman AN, Conley DB, et al. The dilemma of midline destructive lesions: a case series and diagnostic review. 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  9. 9
    Academic Journal

    المصدر: Modern Rheumatology Journal; Том 16, № 5 (2022); 38-45 ; Современная ревматология; Том 16, № 5 (2022); 38-45 ; 2310-158X ; 1996-7012

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Clin Rheumatol. 2010 Sep; 29(9):973-81. doi:10.1007/s10067-010-1496-1. Epub 2010 Jun 30.; Dagna L, Salvo F, Tiraboschi M, et al. Pentraxin-3 as a marker of disease activity in takayasu arteritis. Ann Intern Med. 2011 Oct 4;155(7):425-33. doi:10.7326/0003-4819-155-7-201110040-00005.; Ishihara T, Haraguchi G, Kamiishi T, et al. Sensitive assessment of activity of Takayasu’s arteritis by pentraxin 3, a new biomarker. J Am Coll Cardiol. 2011 Apr 19;57(16):1712-3. doi:10.1016/j.jacc.2010.10.058.; Direskeneli H, Aydin SZ, Merkel PA. Assessment of disease activity and progression in Takayas, s arteritis. Clin Exp Rheumatol. 2011 Jan-Feb;29(1 Suppl 64):S86-91. Epub 2011 May 11.; Sager S, Yilmaz S, Ozhan M, et al. F-18 Fdg PET/CT findings of a patient with Takayasu arteritis before and after therapy. Mol Imaging Radionucl Ther. 2012 Apr;21(1):32-4. doi:10.4274/Mirt.021896. Epub 2012 Apr 1.; Cheng Y, Lv N, Wang Z, et al. 18-FDGPET in assessing disease activity in Takayasu arteritis: a meta-analysis. Clin Exp Rheumatol. 2013 Jan-Feb;31(1 Suppl 75):S22-7. Epub 2013 Feb 25.; Papa M, De Cobelli F, Baldissera E, et al. Takayasu arteritis: intravascular contrast medium for MR angiography in the evaluation of disease activity. AJR Am J Roentgenol. 2012 Mar;198(3):W279-84. doi:10.2214/AJR.11.7360.; Schmidt WA. Imaging in vasculitis. Best Pract Res Clin Rheumatol. 2013 Feb;27(1): 107-18. doi:10.1016/j.berh.2013.01.001.; Zhu FP, Luo S, Wang ZJ, et al. Takayasu arteritis: imaging spectrum at multidetector CT angiography. Br J Radiol. 2012 Dec;85 (1020):e1282-92. doi:10.1259/bjr/25536451.; Arend WP, Michel BA, Bloch DA, et al. The American College of Rheumatology 1990 criteria for the classification of Takayasu arteritis. Arthritis Rheum. 1990 Aug;33(8):1129-34. doi:10.1002/art.1780330811.; Sharma BK, Jain S, Suri S, et al. Diagnostic criteria for Takayasu arteritis. Int J Cardiol. 1996 Aug;54 Suppl:S141-7. doi:10.1016/s0167-5273(96)88783-3.; Misra R, Danda D, Rajappa SM, et al. Development and initial validation of the Indian Takayasu Clinical Activity Score (ITAS2010). Rheumatology (Oxford). 2013 Oct;52(10):1795-801. doi:10.1093/rheumatology/ket128. Epub 2013 Apr 16.; Zoghbi WA , Adams D , Bonow RO . Recommendations for noninvasive evaluation of native valvular regurgitation: a report from the american society of echocardiography developed in collaboration with the society for cardiovascular magnetic resonance. J Am Soc Echocardiogr. 2017Apr;30(4):303-71. doi:10.1016/j.echo.2017.01.007. Epub 2017 Mar 14.; Barnett HJM, Taylor DW, Haynes RB, et al; North American Symptomatic Carotid Endar-erectomy Trial Collaborators. Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade stenosis. N Engl J Med. 1991 Aug 15;325(7):445-53. doi:10.1056/NEJM199108153250701.; Randomised trial of endarterectomy for recently symptomatic carotid stenosis: final results of the MRC European Carotid Surgery Trial (ECST). Lancet. 1998 May 9;351(9113): 1379-87.; Hata A, Noda M, Moriwaki R, et al. Angiographic findings of Takayasu arteritis: new classification. Int J Cardiol. 1996 Aug;54 Suppl:S155-63. doi:10.1016/s0167-5273(96)02813-6.; Jefferson R, Roberts MD. Takayasu Arteritis Differential Diagnoses. Medscape-2016. http://emedicine.medscape.com/article/332378-differential.; Ishikawa K. Natural history and classification of occlusive thromboaortopathy (Takayasu’s disease). Circulation. 1978 Jan;57(1): 27-35. doi:10.1161/01.cir.57.1.27.; Hoffman GS, Ahmed AE. Surrogate markers of disease activity in patients with Takayasu arteritis. A preliminary report from The International Network for the Study of the Systemic Vasculitides (INSSYS). Int J Cardiol. 1998 Oct 1;66 Suppl 1:S191-4; discussion S195. doi:10.1016/s0167-5273(98)00181-8.; Dagna L, Salvo F, Tiraboschi M, et al. Pentraxin-3 as a marker of disease activity in takayasu arteritis. Ann Intern Med. 2011 Oct 4; 155(7):425-33. doi:10.7326/0003-4819-155-7-201110040-00005.; Moriwaki R, Numano F. Takayasu arteritis: follow-up studies for 20 years. Heart Vessels Suppl. 1992;7:138-45. doi:10.1007/BF01744560.; Cieslik P, Hrycek A. Long pentraxin 3 (PTX3) in the light of its structure, mechanism of action and clinical implications. Autoimmunity. 2012 Mar;45(2):119-28. doi:10.3109/08916934.2011.611549. Epub 2011 Oct 11.; Eichhorn J, Sima D, Thiele B, et al. Antiendothelial cell antibodies in Takayasu arteritis. Circulation. 1996 Nov 15;94(10):2396-401. doi:10.1161/01.cir.94.10.2396.; Wang H, Ma J, Wu Q, et al. Circulating B lymphocytes producing autoantibodies to endothelial cells play a role in the pathogenesis of Takayasu arteritis. J Vasc Surg. 2011 Jan; 53(1):174-80. doi:10.1016/j.jvs.2010.06.173. Epub 2010 Sep 15.; Maksimowicz-McKinnon K, Clark TM, Hoffman GS. Limitations of therapy and a guarded prognosis in an American cohort of Takayasu arteritis patients. Arthritis Rheum. 2007 Mar;56(3):1000-9. doi:10.1002/art.22404.; Schneeweis C, Schnackenburg B, Stuber M, et al. Delayed contrast-enhanced MRI of the coronary artery wall in takayasu arteritis. PLoS One. 2012;7(12):e50655. doi:10.1371/journal.pone.0050655. Epub 2012 Dec 7.; Yamada I, Nakagawa T, Himeno Y, et al. Takayasu arteritis: diagnosis with breath-hold contrast-enhanced three-dimensional MR angiography. J Magn Reson Imaging. 2000 May;11(5):481-7. doi:10.1002/(sici)1522-2586(200005)11:53.0.co;2-4.; Eshet Y, Pauzner R, Goitein O, et al. The limited role of MRI in long-term followup of patients with Takayasu’s arteritis. Autoimmun Rev. 2011 Dec;11(2):132-6. doi:10.1016/j.autrev.2011.09.002. Epub 2011 Sep 17.; Yadav MK. Takayasu arteritis: clinical and CT-angiography profile of 25 patients and a brief review of literature. Indian Heart J. 2007 Nov-Dec;59(6):468-74.; Mukhtyar C, Guillevin L, Cid MC, et al. EULAR recommendations for the management of large vessel vasculitis. Ann Rheum Dis. 2009 Mar;68(3):318-23. doi:10.1136/ard.2008.088351. Epub 2008 Apr 15.; https://mrj.ima-press.net/mrj/article/view/1343

  10. 10
    Academic Journal

    المصدر: Modern Rheumatology Journal; Том 16, № 5 (2022); 75-81 ; Современная ревматология; Том 16, № 5 (2022); 75-81 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/1350/1290; Насонов ЕЛ, Баранов АА, Шилкина НП. Васкулиты и васкулопатии. Ярославль: Верхняя Волга; 1999. 616 с.; Theofilis P, Vordoni A, Koukoulaki M, et al. Overview of infections as an etiologic factor and complication in patients with vasculitides. Rheumatol Int. 2022 May;42(5): 759-70. doi:10.1007/s00296-022-05100-9. Epub 2022 Feb 14.; Stegeman CA, Tervaert JW, de Jong PE, Kallenberg CG. Trimethoprim-sulfamethoxazole (co-trimoxazole) for the prevention of relapses of Wegener's granulomatosis. Dutch Co-Trimoxazole Wegener Study Group. N Engl J Med. 1996 Jul 4;335(1):16-20. doi:10.1056/NEJM199607043350103.; Monti S, Delvino P, Riboli M, et al. The role of trimethoprim/sulfametoxazole in reducing relapses and risk of infections in ANCA-associated vasculitis: a meta-analysis. Rheumatology (Oxford). 2021 Aug 2;60(8): 3553-64. doi:10.1093/rheumatology/keab267.; Van Gool IC, Kers J, Bakker JA, et al. Antineutrophil cytoplasmic antibodies in infective endocarditis: a case report and systematic review of the literature. Clin Rheumatol. 2022 Jun 23. doi:10.1007/s10067-022-06240-w. Online ahead of print.; Huan G, Yang G, Xiao-Yu Q, et al. Antineutrophil cytoplasmic antibodies in Chinese patients with tuberculosis. Rev Soc Bras Med Trop. 2018 Jul-Aug;51(4):475-8. doi:10.1590/0037-8682-0400-2017.; Choi H, Park YB, Song J, Lee SW. Unclassifiable repeated antineutrophil cytoplasmic antibody (ANCA) positivity in diseases other than ANCA-associated vasculitis. Z Rheumatol. 2021 Apr 27. doi:10.1007/s00393-021-00998-1. Online ahead of print.; Söderberg D, Segelmark M. Neutrophil Extracellular Traps in ANCA-Associated Vasculitis. Front Immunol. 2016 Jun 30;7:256. doi:10.3389/fimmu.2016.00256.; Xiao H, Hu P, Falk RJ, Jennette JC. Overview of the Pathogenesis of ANCA-Associated Vasculitis. Kidney Dis (Basel). 2016 Mar;1(4): 205-15. doi:10.1159/000442323. Epub 2015 Dec 3.; Lizarraga KJ, Florindez JA, Daftarian P, et al. Anti-GBM disease and ANCA during dengue infection. Clin Nephrol. 2015 Feb; 83(2):104-10. doi:10.5414/CN108217.; Asano S, Mizuno S, Okachi S, et al. Antineutrophil Cytoplasmic Antibody-associated Vasculitis Superimposed on Infection-related Glomerulonephritis Secondary to Pulmonary Mycobacterium avium Complex Infection. Intern Med. 2016;55(17):2439-45. doi:10.2169/internalmedicine.55.6588. Epub 2016 Sep 1.; Addy C, Doran G, Jones AL, et al. Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report. BMC Pulm Med. 2018 Nov 19;18(1):170. doi:10.1186/s12890-018-0732-3.; Hashimoto S, Aizawa T, Watanabe S, et al. Osteomyelitis-related glomerulonephritis with myeloperoxidase-antineutrophil cytoplasmic antibody positivity. Pediatr Int. 2020 Feb; 62(2):236-8. doi:10.1111/ped.14080.; Sugino H, Sawada Y, Nakamura M. IgA Vasculitis: Etiology, Treatment, Biomarkers and Epigenetic Changes. Int J Mol Sci. 2021 Jul 14;22(14):7538. doi:10.3390/ijms22147538.; Абдурахманов ДТ, Розина ТП, Новиков ПИ. HBV-ассоциированный узелковый полиартериит. Эпидемиология и инфекционные болезни. Актуальные вопросы. 2012;(3):67-71.; Семенкова ЕН. Системные некротизирующие васкулиты. Москва: Русский врач; 2001. 96 с.; Игнатова ТМ, Козловская ЛВ, Гордовская НБ, и др. Криоглобулинемический васкулит, ассоциированный с вирусом гепатита С: 20-летний опыт лечения. Терапевтический архив. 2017:(5):45-62.; Vega LE, Espinoza LR. Vasculitides in HIV Infection. Curr Rheumatol Rep. 2020 Aug 26;22(10):60. doi:10.1007/s11926-020-00945-0.; Vega LE, Espinoza LR. Human immunodeficiency virus infection (HIV)-associated rheumatic manifestations in the pre- and post-HAART eras. Clin Rheumatol. 2020 Sep; 39(9):2515-22. doi:10.1007/s10067-020-05082-8. Epub 2020 Apr 15.; Giryes S, Bragazzi NL, Bridgewood C, et al. COVID-19 Vasculitis and vasculopathyDistinct immunopathology emerging from the close juxtaposition of Type II Pneumocytes and Pulmonary Endothelial Cells. Semin Immunopathol. 2022 May;44(3):375-90. doi:10.1007/s00281-022-00928-6. Epub 2022 Apr 12.; Leisman DE, Deutschman CS, Legrand M. Facing COVID-19 in the ICU: vascular dysfunction, thrombosis, and dysregulated inflammation. Intensive Care Med. 2020 Jun; 46(6):1105-8. doi:10.1007/s00134-020-06059-6. Epub 2020 Apr 28.; Брегель ЛВ, Костик ММ, Фелль ЛЗ и др. Болезнь Кавасаки и мультисистемный воспалительный синдром при инфекции COVID-19 у детей. Педиатрия им. Г.Н. Сперанского. 2020;(6):209-19.; Patel P, DeCuir J, Abrams J, et al. Clinical Characteristics of Multisystem Inflammatory Syndrome in Adults: A Systematic Review. JAMA Netw Open. 2021 Sep 1;4(9):e2126456. doi:10.1001/jamanetworkopen.2021.26456.; Fabi M, Filice E, Biagi C, et al. Multisystem Inflammatory Syndrome Following SARS-CoV-2 Infection in Children: One Year after the Onset of the Pandemic in a High-Incidence Area. Viruses. 2021 Oct 7;13(10): 2022. doi:10.3390/v13102022.; Sollini M, Ciccarelli M, Cecconi M, et al. Vasculitis changes in COVID-19 survivors with persistent symptoms: an [18F]FDG-PET/ CT study. Eur J Nucl Med Mol Imaging. 2021 May;48(5):1460-6. doi:10.1007/s00259-020-05084-3.; Morris D, Patel K, Rahimi O, et al. ANCA vasculitis: A manifestation of PostCovid-19 Syndrome. Respir Med Case Rep. 2021;34:101549. doi:10.1016/j.rmcr.2021.101549. Epub 2021 Nov 11.; Cavalli G, Colafrancesco S, De Luca G, et al. Cutaneous vasculitis following COVID-19 vaccination. Lancet Rheumatol. 2021 Nov; 3(11):e743-e744. doi:10.1016/S2665-9913(21)00309-X.; Nappi E, De Santis M, Paoletti G, et al. New Onset of Eosinophilic Granulomatosis with Polyangiitis Following mRNA-Based COVID-19 Vaccine. Vaccines (Basel). 2022 May 3;10(5):716. doi:10.3390/vaccines10050716.; Al-Yafeai Z, Horn BJM, Terraccaine W, et al. A Case of Antineutrophil Cytoplasmic Antibodies (ANCA)-Associated Vasculitis Post COVID-19 Vaccination. Cureus. 2022 Mar 14;14(3):e23162. doi:10.7759/cureus.23162.; Holle JU, Gross WL, Latza U, et al. Improved outcome in 445 patients with Wegener's granulomatosis in a German vasculitis center over four decades. Arthritis Rheum. 2011 Jan;63(1):257-66. doi:10.1002/art.27763.; Cartin-Ceba R, Golbin JM, Keogh KA, et al. Rituximab for remission induction and maintenance in refractory granulomatosis with polyangiitis (Wegener's): ten-year experience at a single center. Arthritis Rheum. 2012 Nov;64(11):3770-8. doi:10.1002/art.34584.; Charlier C, Henegar C, Launay O, et al. Risk factors for major infections in Wegener granulomatosis: analysis of 113 patients. Ann Rheum Dis. 2009 May;68(5):658-63. doi:10.1136/ard.2008.088302.; Aasarød K, Iversen BM, Hammerstrøm J, et al. Wegener's granulomatosis: clinical course in 108 patients with renal involvement. Nephrol Dial Transplant. 2000 May;15(5): 611-8. doi:10.1093/ndt/15.5.611.; Bligny D, Mahr A, Toumelin PL, et al. Predicting mortality in systemic Wegener's granulomatosis: a survival analysis based on 93 patients. Arthritis Rheum. 2004 Feb 15;51(1):83-91. doi:10.1002/art.20082.; Yang L, Xie H, Liu Z, et al. Risk factors for infectious complications of ANCA-associated vasculitis: a cohort study. BMC Nephrol. 2018 Jun 14;19(1):138. doi:10.1186/s12882-018-0933-2.; Kronbichler A, Jayne DR, Mayer G. Frequency, risk factors and prophylaxis of infection in ANCA-associated vasculitis. Eur J Clin Invest. 2015 Mar;45(3):346-68. doi:10.1111/eci.12410.; Jung M, Barra L. Rate of infections in severe necrotising vasculitis patients treated with cyclophosphamide induction therapy: a metaanalysis. Clin Exp Rheumatol. 2018 Mar-Apr; 36 Suppl 111(2):129-34.; Yates M, Watts RA, Bajema IM, et al. EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis. Ann Rheum Dis. 2016 Sep;75(9):1583-94. doi:10.1136/annrheumdis-2016-209133; Segelmark L, Flores-Suarez L, Mohammad A. Severe infections in patients with ANCA-associated vasculitis treated with rituximab. Rheumatology (Oxford). 2021 Dec 24;61(1):205-12. doi:10.1093/rheumatology/keab293.; Odler B, Windpessl M, Krall M, et al. The Risk of Severe Infections Following Rituximab Administration in Patients With Autoimmune Kidney Diseases: Austrian ABCDE Registry Analysis. Front Immunol. 2021 Oct 29;12:760708. doi:10.3389/fimmu.2021.760708. eCollection 2021.; Lee YH, Song GG. Comparative efficacy and safety of rituximab, mycophenolate, methotrexate, and cyclophosphamide versus azathioprine as maintenance therapy in antineutrophil cytoplasmic antibody-associated vasculitis: A Bayesian network meta-analysis of randomized controlled trials. Int J Clin Pharmacol Ther. 2022 Feb;60(2):97-105. doi:10.5414/CP204053.; Furuta S, Nakagomi D, Kobayashi Y, et al. Effect of Reduced-Dose vs High-Dose Glucocorticoids Added to Rituximab on Remission Induction in ANCA-Associated Vasculitis: A Randomized Clinical Trial. JAMA. 2021 Jun 1;325(21):2178-87. doi:10.1001/jama.2021.6615.; Godeau B, Mainardi JL, Roudot-Thoraval F, et al. Factors associated with Pneumocystis carinii pneumonia in Wegener's granulomatosis. Ann Rheum Dis. 1995 Dec; 54(12):991-4.; Ognibene FP, Shelhamer JH, Hoffman GS, et al. Pneumocystis carinii pneumonia: a major complication of immunosuppressive therapy in patients with wegener’s granulomatosis. Am J Respir Crit Care Med. 1995 Mar;151 (3 Pt 1):795-9. doi:10.1164/ajrccm/151.3_Pt_1.795.; Falagas ME, Manta KG, Betsi GI, et al. Infection-related morbidity and mortality in patients with connective tissue diseases: a systemic review. Clin Rheumatol. 2007 May;26(5): 663-70. doi:10.1007/s10067-006-0441-9. Epub 2006 Dec 21.; Fillatre P, Decaux O, Jouneau S, et al. Incidence of Pneumocystis jiroveci pneumonia among groups at risk in HIV-negative patients. Am J Med. 2014 Dec;127(12):1242.e11- 7. doi:10.1016/j.amjmed.2014.07.010. Epub 2014 Jul 21.; Li J, Huang XM, Fang WG, et al. Pneumocystis carinii pneumonia in patients with connective tissue disease. J Clin Rheumatol. 2006 Jun;12(3):114-7. doi:10.1097/01.rhu.0000221794.24431.36.; Zhang Y, Zheng Y. Pneumocystis jirovecii pneumonia in mycophenolate mofetil-treated patients with connective tissue disease: analysis of 17 cases. Rheumatol Int. 2014 Dec; 34(12):1765-71. doi:10.1007/s00296-014-3073-4. Epub 2014 Jun 20.; Guillevin L, Cordier JF, Lhote F, et al. A prospective, multicenter, randomized trial comparing steroids and pulse cyclophosphamide versus steroids and oral cyclophosphamide in the treatment of generalized wegener’s granulomatosis. Arthritis Rheum. 1997 Dec;40(12):2187-98. doi:10.1002/art.1780401213.; Jones RB, Tervaert JWC, Hauser T, et al. Rituximab versus cyclophosphamide in ANCA-associated renal vasculitis. N Engl J Med. 2010 Jul 15;363(3):211-20. doi:10.1056/NEJMoa0909169.; Specks U, Merkel PA, Seo P, et al. Efficacy of remission-induction regimens for ANCA-associated vasculitis. N Engl J Med. 2013 Aug 1;369(5):417-27. doi:10.1056/NEJMoa1213277.; Guillevin L, Pagnoux C, Karras A, et al. Rituximab versus azathioprine for maintenance in ANCA-associated vasculitis. N Engl J Med. 2014 Nov 6;371(19):1771-80. doi:10.1056/NEJMoa1404231.; Chung SA, Langford CA, Maz M, et al. 2021 American College of Rheumatology/ Vasculitis Foundation Guideline for the Management of Antineutrophil Cytoplasmic Antibody-Associated Vasculitis. Arthritis Rheumatol. 2021 Aug;73(8):1366-83. doi:10.1002/art.41773. Epub 2021 Jul 8.; Chung JB, Armstrong K, Schwartz S, et al. Cost-effectiveness of prophylaxis against pneumocystis carinii pneumonia in patients with wegener’s granulomatosis undergoing immunosuppressive therapy. Arthritis Rheum. 2000 Aug;43(8):1841-8. doi:10.1002/1529-0131(200008)43:83.0.CO;2-Q.; Sattui SE, Conway R, Putman MS, et al. Outcomes of COVID-19 in patients with primary systemic vasculitis or polymyalgia rheumatica from the COVID-19 Global Rheumatology Alliance physician registry: a retrospective cohort study. Lancet Rheumatol. 2021 Dec;3(12):e855-e864. doi:10.1016/S2665-9913(21)00316-7. Epub 2021 Nov 5.; Machado PM, Lawson-Tovey S, Strangfeld A, et al. Safety of vaccination against SARS-CoV-2 in people with rheumatic and musculoskeletal diseases: results from the EULAR Coronavirus Vaccine (COVAX) physician-reported registry. Ann Rheum Dis. 2022 May;81(5):695-709. doi:10.1136/annrheumdis-2021-221490. Epub 2021 Dec 31.; David R, Hanna P, Lee K, Ritchie A. Relapsed ANCA associated vasculitis following Oxford AstraZeneca ChAdOx1-S COVID-19 vaccination: A case series of two patients. Nephrology (Carlton). 2022 Jan; 27(1):109-10. doi:10.1111/nep.13993. Epub 2021 Nov 9.; Kondo M, Yamanaka K. Possible HSP reactivation post-COVID-19 vaccination and booster. Clin Case Rep. 2021 Oct 28;9(10): e05032. doi:10.1002/ccr3.5032. eCollection 2021 Oct.; Dharia T, Venkatachalam S, Baker JF, et al. Medication Interruptions and Subsequent Disease Flares During the COVID-19 Pandemic: A Longitudinal Online Study of Patients With Rheumatic Disease. Arthritis Care Res (Hoboken). 2022 May;74(5):733-40. doi:10.1002/acr.24837.; Chen YX, Yu HJ, Zhang W, et al. Analyzing fatal cases of Chinese patients with primary antineutrophil cytoplasmic antibodiesassociated renal vasculitis: a 10-year retrospective study. Kidney Blood Press Res. 2008; 31(5):343-9. doi:10.1159/000165117. Epub 2008 Oct 23.; Itabashi M, Takei T, Yabuki Y, et al. Clinical outcome and prognosis of anti-neutrophil cytoplasmic antibody-associated vasculitis in Japan. Nephron Clin Pract. 2010;115(1):c21-7. doi:10.1159/000286346. Epub 2010 Feb 19.; Flossmann O, Berden A, de Groot K, et al. Long-term patient survival in ANCAassociated vasculitis. 2011 Mar;70(3):488-94. doi:10.1136/ard.2010.137778.; https://mrj.ima-press.net/mrj/article/view/1350

  11. 11
    Academic Journal

    المساهمون: The investigation has been conducted within scientific topic "Innovative technologies for the diagnosis and treatment of systemic diseases of the connective tissue" (IKBRS 0397-2020-0006)., Работа выполнена в рамках научной исследовательской работы «Инновационные технологии диагностики и лечения системных заболеваний соединительной ткани» (ИКБРС 0397-2020-0006).

    المصدر: Modern Rheumatology Journal; Том 16, № 4 (2022); 21-26 ; Современная ревматология; Том 16, № 4 (2022); 21-26 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/1318/1264; Molina-Ruiz AM, Requena L. Erythema nodosum. Med Clin (Barc). 2016;147(2):81-6. doi:10.1016/j.medcli.2016.03.038; Mert A, Kumbasar H, Ozaras R, et al. Erythema nodosum: an evaluation of 100 cases. Clin Exp Rheumatol. Jul-Aug 2007; 25(4):563-70.; Cox NH, Jorizzo JL, Bourke JF, Savage COS. Vasculitis, Neutrophilic Dermatoses and Related Disorders. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook’s Textbook of Dermatology. 8th edition. Vol. 1. Wiley; 2010. P. 82-7.; Elkayam O, Caspi D, Segal R, et al. Familial erythema nodosum. Arthritis Rheum. 1991 Sep;34(9):1177-9. doi:10.1002/art.1780340915.; Labunski S, Posern G, Ludwig S, et al. Tumour necrosis factor-alpha promoter polymorphism in erythema nodosum. Acta Derm Venereol. Jan-Feb 2001;81(1):18-21. doi:10.1080/00015550116912.; Amoli MM, Ollier WER, Lueiro M, et al. Lack of association between ICAM-1 gene polymorphisms and biopsy-proven erythema nodosum. J Rheumatol. 2004 Feb;31(2):403-5.; Zheng W, Song W, Wu Q, et al. Analysis of the clinical characteristics of thirteen patients with Weber–Christian panniculitis. Clin Rheumatol. 2019 Dec;38(12):3635-41. doi:10.1007/s10067-019-04722-y. Epub 2019 Aug 12.; Akdis AC, Kilicturgay K, Helvaci S, et al. Immunological evaluation of erythema nodosum in tularaemia. Br J Dermatol. 1993 Sep; 129(3):275-9. doi:10.1111/j.1365-2133.1993.tb11846.x.; Егорова ОН, Белов БС, Глухова СИ, Раденска-Лоповок СГ. Идиопатический лобулярный панникулит как общеклиническая проблема. Терапевтический архив. 2019;91(5):49-53.; Сахарова КВ, Черкасова МВ, Эрдес ШФ. Сывороточный амилоид А как маркер активности анкилозирующего спондилита. Современная ревматология. 2021;15(6):72-5. doi:10.14412/1996-7012-2021-6-72-75.; Hwang YG, Balasubramani GK, Metes ID, et al. Differential response of serum amyloid A to different therapies in early rheumatoid arthritis and its potential value as a disease activity biomarker. Arthritis Res Ther. 2016 May 17;18(1):108. doi:10.1186/s13075-016-1009-y.; Sun L, Ye RD. Serum Amyloid A1: Structure, Function and Gene Polymorphism. Gene. 2016 May 25;583(1):48-57. doi:10.1016/j.gene.2016.02.044. Epub 2016 Mar 3.; Крылов МЮ, Егорова ОН, Белов БС. Генетические аспекты панникулитов в российской популяции (пилотное исследование). Научно-практическая ревматология. 2016;54(5):553-6.; De Simone C, Caldarola G, Scaldaferri F, et al. Clinical, histopathological, and immunological evaluation of a series of patients with erythema nodosum. Int J Dermatol. 2016 May; 55(5):e289-94. doi:10.1111/ijd.13212. Epub 2016 Feb 24.; Frucht DM, Aringer M, Galon J, et al. Stat4 is expressed in activated peripheral blood monocytes, dendritic cells, and macrophages at sites of Th1-mediated inflammation. J Immunol. 2000 May 1;164(9):4659-64. doi:10.4049/jimmunol.164.9.4659.; Watford WT, Hissong BD, Bream JH, et al. Signaling by IL-12 and IL-23 and the immunoregulatory roles of STAT4. Immunol Rev. 2004 Dec;202:139-56. doi:10.1111/j.0105-2896.2004.00211.x.; https://mrj.ima-press.net/mrj/article/view/1318

  12. 12
    Academic Journal

    المساهمون: The investigation has been conducted within scientific topic №0397-2020-0006 «Innovative technologies for the diagnosis and treatment of systemic connective tissue diseases»., Работа выполнена в рамках научной исследовательской работы «Инновационные технологии диагностики и лечения системных заболеваний соединительной ткани» (ИКБРС 0397-2020-0006).

    المصدر: Modern Rheumatology Journal; Том 16, № 1 (2022); 84-90 ; Современная ревматология; Том 16, № 1 (2022); 84-90 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/1257/1215; Вербенко ЕВ. Спонтанный панникулит. Вкн: Скрипкин ЮК, редактор. Кожные и венерические болезни. Руководство для врачей. Москва: Медицина; 1995. С. 399-410.; Diaz CC, Borghi S, Weyers W. Panniculitis: definition of terms and diagnostic strategy. Am J Dermatopathol. 2000 Dec;22(6):530-49. doi:10.1097/00000372-200012000-00009.; Requena L, Yus ES. Panniculitis. Part I. Mostly septal panniculitis. J Am Acad Dermatol. 2001 Aug;45(2):163-83; quiz 184-6. doi:10.1067/mjd.2001.114736.; Requena L, Sanchez Yus E. Panniculitis. Part II. Mostly lobular panniculitis. J Am Acad Dermatol. 2001 Sep;45(3):325-61; quiz 362-4. doi:10.1067/mjd.2001.114735.; Wick MR. Panniculitis: A summary. Semin Diagn Pathol. 2017 May;34(3):261-72. doi:10.1053/j.semdp.2016.12.004. Epub 2016 Dec 27.; Caputo V, Rongioletti F. Panniculitis in the setting of dermato/rheumatologic diseases. G Ital Dermatol Venereol. 2018 Apr;153(2): 194-207. doi:10.23736/S0392-0488.17.05845-X. Epub 2017 Dec 15.; Егорова ОН, Белов БС. Панникулиты в практике дерматовенеролога и интерниста. Consilium Medicum. 2020;22(7):78-83.; Elder DE, Elenitsas R, Rosenbach M, et al. Lever’s histopathology of the skin. 11th edition. Philadelphia : Wolters Kluwer; 2014. P. 952-1009.; Hansen CB, Callen JP. Connective tissue panniculitis: lupus panniculitis, dermatomyositis, morphea/scleroderma. Dermatol Ther. Jul-Aug 2010;23(4):341-9. doi:10.1111/j.1529-8019.2010.01334.x.; Binesh VG, Krishnan J, Asokan N, Ajithkumar K. Systemic sclerosis presenting as lobular panniculitis. Indian Dermatol Online J. 2012 Sep;3(3):222-4. doi:10.4103/2229-5178.101830.; Hasegawa A, Shimomura Y, Kibune N, et al. Panniculitis as the initial manifestation of dermatomyositis with anti-MDA5 antibody. Clin Exp Dermatol. 2017 Jul;42(5):551-3. doi:10.1111/ced.13128. Epub 2017 May 22.; Бекетова ТВ, Насонов ЕЛ. Инновационные методы лечения артериита Такаясу: в фокусе ингибиторы интерлейкина 6. Собственный опыт применения тоцилизумаба и обзор литературы. Научно-практическая ревматология. 2017;55(5): 536-48.; Velter C, Lipsker D. Cutaneous panniculitis. Rev Med Interne. 2016 Nov;37(11):743-50. doi:10.1016/j.revmed.2016.05.008. Epub 2016 Jun 16.; Раденска-Лоповок СГ, Егорова ОН, Белов БС и др. Идиопатический лобулярный панникулит: клинико-морфологические корреляции. Архив патологии. 2019; 81(3):37-44.; Lin F, Prichard J. Handbook of practical immunohistochemistry: Frequently asked questions. New York: Springer Science+ Business Media; 2015. P. 17-31.; Winkelmann RK, Peters MS. Lupus panniculitis. Dermatology update. New York: Elsevier; 1982. P. 135-52.; Martens PB, Moder KG, Ahmed I. Lupus panniculitis: clinical perspectives from a case series. J Rheumatol. 1999 Jan;26(1):68-72.; Sudhakar P, Shah GV, Saponara F, et al. Central retinal artery occlusion secondary to orbital inflammation in lupus erythematosus profundus. J Neuroophthalmol. 2012 Mar;32(1): 93-4. doi:10.1097/WNO.0b013e31823f8548.; Lueangarun S, Subpayasarn U, Tempark T. Distinctive lupus panniculitis of scalp with linear alopecia along Blaschko's lines: a review of the literature. Int J Dermatol. 2019 Feb; 58(2):144-50. doi:10.1111/ijd.14155. Epub 2018 Aug 3.; Navarro-Triviсo FJ, Ortego Centeno N. Linear lupus panniculitis of the scalp with good response to thalidomide. Lupus. 2019 Oct;28(11):1380-2. doi:10.1177/0961203319873703. Epub 2019 Sep 10.; Rangel LK, Villa-Ruiz C, Lo K, et al. Clinical Characteristics of Lupus Erythematosus Panniculitis/Profundus: A Retrospective Review of 61 Patients. JAMA Dermatol. 2020 Nov 1;156(11):1264-6. doi:10.1001/jamadermatol.2020.2797.; Filotico R, Mastrandrea V. Cutaneous lupus erythematosus: clinico-pathologic correlation. G Ital Dermatol Venereol. 2018 Apr; 153(2):216-29. doi:10.23736/S0392-0488.18.05929-1. Epub 2018 Jan 24.; Fraga J, Garcнa-Dнez A. Lupus erythematosus panniculitis. Dermatol Clin. 2008 Oct; 26(4):453-63, vi. doi:10.1016/j.det.2008.06.002.; Tuffanelli DL. Lupus erythematosus (panniculitis) profundus: a classic revisited commentary and report of 22 cases. Hawaii Med J. 1982 Nov;41(11):394-7.; Насонов ЕЛ, редактор. Ревматология. Российские клинические рекомендации. Москва: ГЭОТАР-Медиа; 2017. С. 113-36.; Gladman DD, Goldsmith CH, Urowitz MB, et al. The Systemic Lupus Ery-thematosus Collaborating Clinics. American College of Rheumatology index for systemic lupus erythematosus international comparison. J Rheumatol.2000 Feb;27(2):373-6.; Peters MS, Su WP. Eosinophils in lupus panniculitis and morphea profunda. J Cutan Pathol. 1991 Jun;18(3):189-92. doi:10.1111/j.1600-0560.1991.tb00151.x.; Gonzalez-Cruz C, Aparicio Espaсol G, Ferrer Fаbrega B, et al. Lupus panniculitis: Clinicopathological features of a series of 12 patients. Med Clin (Barc). 2018 Dec 14; 151(11):444-9. doi:10.1016/j.medcli.2018.06.024. Epub 2018 Aug 25.; Wang T, Li X, Liu YH, et al. Lupus erythematosus panniculitis: clinical and histopathological analysis of 22 cases. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2011 Oct;33(5):525-8.; Massone C, Kodama K, Salmhofer W, et al. Lupus erythematosus panniculitis (lupus profundus): clinical, histopathological, and molecular analysis of nine cases. J Cutan Pathol. 2005 Jul;32(6):396-404. doi:10.1111/j.0303-6987.2005.00351.x.; Park HS, Choi JW, Kim BK, Cho KH. Lupus erythematosus panniculitis: clinicopathological, immunophenotypic, and molecular studies. Am J Dermatopathol. 2010 Feb;32(1): 24-30. doi:10.1097/DAD.0b013e3181b4a5ec.; Лила АМ, Мазуров ВИ, Лапин СВ и др. Современные возможности ранней диагностики системной красной волчанки. Современная ревматология. 2018;12(3):34-9.; Mysorekar VV, Sumathy TK, Shyam Prasad AL. Role of direct immunofluorescence in dermatological disorders. Indian Dermatol Online J. May-Jun 2015;6(3):172-80. doi:10.4103/2229-5178.156386.; Sontheimer RD, Gilliam JN. A reappraisal of the relationship between subepidermal immunoglobulin deposits and DNA antibodies in systemic lupus erythematosus: a study using the Crithidia luciliae immunofluorescence anti-DNA assay. J Invest Dermatol. 1979 Jan;72(1):29-32. doi:10.1111/1523-1747.ep12530158.; Carvalho MF, Coelho RA. Lupus band test: diagnostic value in disseminated lupus erythematosus. Acta Med Port. Sep-Oct 1991; 4(5):242-8.; Carroll M, Mellick N, Wagner G. Dermatomyositis panniculitis: a case report. Australas J Dermatol. 2015 Aug;56(3):224-6. doi:10.1111/ajd.12172. Epub 2014 Apr 1.; Антелава ОА, Егорова ОН, Белов БС и др. Панникулит при дерматомиозите. Научно-практическая ревматология. 2016;54(2):227-32.; Solons R, Cortes J, Selva A, et al. Panniculitis: a cutaneous manifestation of dermatomyositis. J Am Acad Dermatol. 2002 May; 46(5 Suppl):S148-50. doi:10.1067/mjd.2002.107491.; Rivas OMM, Villa VA, Lara GL, et al. Panniculitis in juvenile dermatomyositis. Clin Exp Dermatol. 2015 Jul;40(5):574-5. doi:10.1111/ced.12576. Epub 2015 Feb 16.; Salman A, Kasapcopur O, Ergun T, et al. Panniculitis in juvenile dermatomyositis: Report of a case and review of the published work. J Dermatol. 2016;43(8):951-3.; Arias M, Hernandez MI, Cunha LG, Kien MC, Abeldaсo A. Panniculitis in a patient with dermatomyositis. An Bras Dermatol. Jan-Feb 2011;86(1):146-8. doi:10.1590/s0365-05962011000100023.; Azevedo PO, Castellen NR, Salai AF, et al. Panniculitis associated with amyopathic dermatomyositis. An Bras Dermatol. Jan-Feb 2018;93(1):119-21. doi:10.1590/abd1806-4841.20186597.; Calle A, La Fe P. Dermatomyositis panniculitis: A case series and review of the literature. JAAD 2018;104(79):3. doi:10.1016/j.jaad.2018.05.445; Bisht A, Parajuli N, Vaidya M, Tiwari S. Panniculitis as an Initial Presentation of Dermatomyositis: A Case Report. JNMA J Nepal Med Assoc. 2020 Mar;58(223):181-4. doi:10.31729/jnma.4827.; Santos-Briz A, Calle A, Linos K, et al. Dermatomyositis panniculitis: a clinicopathological and immunohistochemical study of 18 cases. J Eur Acad Dermatol Venereol. 2018 Aug;32(8):1352-9. doi:10.1111/jdv.14932. Epub 2018 Mar 27.; Pinto AS, Santos FC, Dinis SP, et al. Painful erythematoviolaceous nodules in dermatomyositis. Rheumatology (Oxford). 2021 Mar 2;60(3):1573-4. doi:10.1093/rheumatology/keaa455.; Хаитов РМ. Иммунология: структура и функции иммунной системы. Москва: ГЭОТАР-Медиа; 2019. С. 155-60.; Oon S, Monaghan K, Ng M, et al. A potential association between IL-3 and type I and III interferons in systemic lupus erythematosus. Clin Transl Immunology. 2019 Dec 24;8(12):e01097. doi:10.1002/cti2.1097.eCollection 2019.; Leonard D, Eloranta ML, Hagberg N, et al. Activated T cells enhance interferonproduction by plasmacytoid dendritic cells stimulated with RNA-containing immune complexes. Ann Rheum Dis. 2016 Sep;75(9): 1728-34. doi:10.1136/annrheumdis-2015-208055. Epub 2015 Oct 22.; McNiff JM, Kaplan DH. Plasmacytoid dendritic cells are present in cutaneous dermatomyositis lesions in a pattern distinct from lupus erythematosus. J Cutan Pathol. 2008 May;35(5):452-6. doi:10.1111/j.1600-0560.2007.00848.x. Epub 2007 Nov 12.; https://mrj.ima-press.net/mrj/article/view/1257

  13. 13
    Academic Journal

    المساهمون: The investigation has been conducted within scientific research work "Innovative technologies for the diagnosis and treatment of systemic diseases of the connective tissue" (IKBRS 0397-2020-0006)., Работа выполнена в рамках научной исследовательской работы «Инновационные технологии диагностики и лечения системных заболеваний соединительной ткани» (ИКБРС 0397-2020-0006).

    المصدر: Modern Rheumatology Journal; Том 16, № 3 (2022); 103-109 ; Современная ревматология; Том 16, № 3 (2022); 103-109 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    Relation: https://mrj.ima-press.net/mrj/article/view/1306/1258; Hoeger Р, Kinsler V, Yan A, et al. Harper's Textbook of Pediatric Dermatology. 4th ed. John Wiley & Sons Ltd.; 2020. P. 1207-20.; Wick MR. Panniculitis: A summary. Semin Diagn Pathol. 2017 May;34(3):261-72. doi:10.1053/j.semdp.2016.12.004. Epub 2016 Dec 27.; Caputo V, Rongioletti F. Panniculitis in the setting of dermato/rheumatologic diseases. G Ital Dermatol Venereol. 2018 Apr;153(2): 194-207. doi:10.23736/S0392-0488.17.05845-X. Epub 2017 Dec 15.; Мусатов ИД, Раденска-Лоповок СГ, Егорова ОН, Коломейчук АА. Морфологические особенности лобулярного панникулита при системной красной волчанке и дерматомиозите. Современная ревматология. 2022;16(1):84-90.; Velter C, Lipsker D. Cutaneous panniculitis. Rev Med Interne. 2016 Nov;37(11):743-50. doi:10.1016/j.revmed.2016.05.008. Epub 2016 Jun 16.; Раденска-Лоповок СГ, Егорова ОН, Белов БС и др. Идиопатический лобулярный панникулит: клинико-морфологические корреляции. Архив патологиию 2019; 81(3):37-44.; Del Pozzo Magana BR, Ho N. Subcutaneous fat necrosis of the newborn: a 20 year retrospective study. Pediatr Dermatol. 2016 Nov; 33(6):e353-e355. doi:10.1111/pde.12973. Epub 2016 Aug 30.; Lara LG, Villa AV, Rivas MM, et al. Subcutaneous fat necrosis of the newborn: report of five cases. Pediatr Neonatol. 2017 Feb;58(1): 85-8. doi:10.1016/j.pedneo.2014.06.010. Epub 2014 Nov 26.; Stefanko NS, Drolet BA. Subcutaneous fat necrosis of the newborn and associated hypercalcemia: a systematic review of the literature. Pediatr Dermatol. 2019 Jan;36(1):24-30. doi:10.1111/pde.13640. Epub 2018 Sep 6.; Zeb A, Darmstadt GL. Sclerema neonatorum: a review of nomenclature, clinical presentation, histological features, differential diagnoses and management. J Perinatol. 2008 Jul;28(7):453-60. doi:10.1038/jp.2008.33. Epub 2008 Mar 27.; Buster KJ, Burford HN, Stewart FA, et al. Sclerema neonatorum treated with intravenous immunoglobulin: a case report and review of treatments. Cutis. 2013 Aug;92(2):83-7.; Quesada Cortes A, Campos Munoz L, Diaz Diaz RM, Casado Jimenez M. Cold panniculitis. Dermatol Clin 2008;26:485–9, vii; Ohmura K. Nakajo-Nishimura syndrome and related proteasome-associated autoinflammatory syndromes. J Inflamm Res. 2019 Sep 17;12:259-65. doi:10.2147/JIR.S194098. eCollection 2019.; Федоров ЕС, Салугина СО, Кузьмина НН. Развитие учения об аутовоспалительных заболеваниях в XXI веке. Научно-практическая ревматология 2018;56(4):5-18.; Polat A, Dinulescu M, Fraitag S, et al. Skin manifestations among GATA2-deficient patients. Br J Dermatol. 2018 Mar;178(3):781-5. doi:10.1111/bjd.15548. Epub 2017 Oct 11.; Spinner MA, Sanchez LA, Hsu AP, et al. GATA2 deficiency: A protean disorder of hematopoiesis, lymphatics, and immunity. Blood. 2014 Feb 6;123(6):809-21. doi:10.1182/blood-2013-07-515528. Epub 2013 Nov 13.; Chasset F, Fayand A, Moguelet P, et al. Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational study. J Am Acad Dermatol. 2020 Dec;83(6): 1794-8. doi:10.1016/j.jaad.2020.03.110. Epub 2020 Apr 10.; Shwin KW, Lee CR, Goldbach-Mansky R. Dermatologic Manifestations of Monogenic Autoinflammatory Diseases. Dermatol Clin. 2017 Jan;35(1):21-38. doi:10.1016/j.det.2016.07.005.; Luchsinger I, Coulombe J, Rongioletti F, et al. Self-healing juvenile cutaneous mucinosis: Clinical and histopathologic findings of 9 patients: The relevance of long-term followup. J Am Acad Dermatol. 2018 Jun;78(6): 1164-70. doi:10.1016/j.jaad.2017.10.023. Epub 2017 Oct 21.; Егорова ОН, Белов БС. Панникулиты в практике дерматовенеролога и интерниста. Consilium Medicum. 2020;22(7):78-83.; Mills L, Randall MM. Disseminated coccidioidomycosis presenting as fever of unknown origin and erythema nodosum in a 3-year-old child. Case Rep Pediatr. 2021 Oct 15;2021:1755163. doi:10.1155/2021/1755163. eCollection 2021.; Jang HJ, Suh HR, Choi S, et al. Severe disease activity based on the paris classification is associated with the development of extraintestinal manifestations in korean children and adolescents with ulcerative colitis. J Korean Med Sci. 2021 Nov 15;36(44):e278. doi:10.3346/jkms.2021.36.e278.; Федоров ЕС, Каменец ЕА, РаденскаЛоповок СГ и др. Синдром Блау или саркоидоз с ранним началом. Педиатрия. 2016; 95(3):86-94.; Saghir S, Meskini T, Ettair S, et al. Weber-Christian's disease: a preleukemic disorder? Pan Afr Med J. 2019 Mar 18;32:127. doi:10.11604/pamj.2019.32.127.16106.; El Masnaoui N, Boujemaa Y, Asermouh A, et al. La maladie de Weber-Christian chez un nourrisson: а propos d'une observation. Journal de Pediatrie et de Puericulture. 2010;23:272-4.; Попов ИВ, Быстров АВ, Гамаюнов БН, Сучкова ТН. Панникулит Пфейфера Вебера Крисчена (Клиническое наблюдение). Детская больница. 2010;(1):38-40.; Егорова ОН, Белов БС, Глухова СИ, Раденска-Лоповок СГ. Идиопатический лобулярный панникулит как общеклиническая проблема. Терапевтический архив. 2019;91(5):49-53.; Noh G, Han CW. Intravenous immune globulin therapy after unsuccessful treatment with corticosteroid and cyclosporine a in Pfeifer-Weber-Christian disease: a case report. Am J Case Rep. 2021 Jan 4; 22:e929519. doi:10.12659/AJCR.929519.; Asano Y, Idezuki T, Igarashi A. A case of Rothmann-Makai panniculitis successfully treated with tetracycline. Clin Exp Dermatol. 2006 May;31(3):365-7. doi:10.1111/j.1365-2230.2005.02055.x.; Матвеева СА. Диагноз панникулита Ротмана-Макаи. Клин Мед (Моск). 1994; 72(3):52-3.; Levy J, Burnett ME, Magro CM. Lipophagic Panniculitis of Childhood: A Case Report and Comprehensive Review of the Literature. Am J Dermatopathol. 2017 Mar;39(3): 217-24. doi:10.1097/DAD.0000000000000721.; Sanmartin O, Requena C, Requena L. Factitial panniculitis. 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    المصدر: Modern Rheumatology Journal; Том 15, № 4 (2021); 31-37 ; Современная ревматология; Том 15, № 4 (2021); 31-37 ; 2310-158X ; 1996-7012

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    المصدر: Modern Rheumatology Journal; Том 15, № 3 (2021); 75-80 ; Современная ревматология; Том 15, № 3 (2021); 75-80 ; 2310-158X ; 1996-7012

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    المصدر: Modern Rheumatology Journal; Том 15, № 2 (2021); 77-82 ; Современная ревматология; Том 15, № 2 (2021); 77-82 ; 2310-158X ; 1996-7012

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    المصدر: Modern Rheumatology Journal; Том 15, № 1 (2021); 105-110 ; Современная ревматология; Том 15, № 1 (2021); 105-110 ; 2310-158X ; 1996-7012

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    Academic Journal

    المساهمون: The investigation has been conducted within scientific topic №0397-2020-0006 «Innovative technologies for the diagnosis and treatment of systemic connective tissue diseases»., Работа выполнена в рамках научной исследовательской работы «Инновационные технологии диагностики и лечения системных заболеваний соединительной ткани» (ИКБРС 0397-2020-0006).

    المصدر: Modern Rheumatology Journal; Том 15, № 5 (2021); 108-113 ; Современная ревматология; Том 15, № 5 (2021); 108-113 ; 2310-158X ; 1996-7012

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  19. 19
    Academic Journal

    المصدر: Modern Rheumatology Journal; Том 14, № 1 (2020); 57-61 ; Современная ревматология; Том 14, № 1 (2020); 57-61 ; 2310-158X ; 1996-7012 ; 10.14412/1996-7012-2020-1

    وصف الملف: application/pdf

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  20. 20
    Academic Journal

    المساهمون: The investigation was conducted as part of the research «Comorbid infections in rheumatic diseases and the safety problems of antirheumatic therapy» (AAAA-A19-119021190148-3, 0514-2019-0005) and the applied research «Innovative technologies for the diagnosis and treatment of systemic connective tissue diseases» (0597-2020-0006)., Работа выполнена в рамках научной исследовательской работы «Коморбидные инфекции при ревматических заболеваниях и проблемы безопасности антиревматической терапии» (АААА-А19-119021190148-3, 0514-2019-0005) и прикладного научного исследования «Инновационные технологии диагностики и лечения системных заболеваний соединительных тканей» (0597-2020-0006).

    المصدر: Modern Rheumatology Journal; Том 14, № 2 (2020); 35-40 ; Современная ревматология; Том 14, № 2 (2020); 35-40 ; 2310-158X ; 1996-7012 ; 10.14412/1996-7012-2020-2

    وصف الملف: application/pdf

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