Academic Journal

From membranoproliferative glomerulonephritis to a final diagnosis: Hypocomplementemic urticarial vasculitis syndrome

التفاصيل البيبلوغرافية
العنوان: From membranoproliferative glomerulonephritis to a final diagnosis: Hypocomplementemic urticarial vasculitis syndrome
المؤلفون: Joana Marques, Tiago Pereira, Dulce Carvalho, Mário Góis, Helena Sousa, Francisco Ribeiro, Fernando Nolasco
المصدر: Revista Portuguesa de Nefrologia e Hipertensão, Vol 35, Iss 4, Pp 254-259 (2021)
بيانات النشر: Publicações Ciência e Vida, 2021.
سنة النشر: 2021
المجموعة: LCC:Pathology
مصطلحات موضوعية: membranoproliferative glomerulonephritis, urticaria, hypocomplementemia, hypocomplementemic urticarial vasculitis syndrome, systemic lupus erythematosus, anti-c1q antibodies, Pathology, RB1-214
الوصف: Membranoproliferative glomerulonephritis describes a glomerular-injury pattern common to a heterogeneous group of diseases. Evaluation based on clinical and laboratory presentation and immunofluorescence staining on kidney biopsy allows identification of underlying pathophysiological processes and may facilitate proper diagnosis and treatment. Hypocomplementemic urticarial vasculitis syndrome is a rare autoimmune disease of multi-organ involvement. The diagnosis is based on well-defined clinical and laboratory criteria. The pathophysiology is not completely understood but the presence of anti-C1q antibody seems to be involved. Renal involvement occurs in up to 50% of cases. It can be heterogeneous and can be indistinguishable from lupus nephritis. Serological findings and skin involvement distinguish these two entities. We report the case of a 40-year-old female who presented with urticarial skin lesions, hypocomplementemia and nephrotic syndrome. Kidney biopsy showed membranoproliferative glomerulonephritis with full house immune complex deposits. The diagnosis of hypocomplementemic urticarial vasculitis syndrome was made and the patient was successfully treated with prednisolone and mycophenolate mofetil.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0872-0169
2183-1289
Relation: http://www.bbg01.com/cdn/rsc/spnefro/advaccess/335/11Nefro354CASE2.pdf; https://doaj.org/toc/0872-0169; https://doaj.org/toc/2183-1289
DOI: 10.32932/pjnh.2021.12.161
URL الوصول: https://doaj.org/article/8ea4b556b83348028b6edeeaaa2e5f33
رقم الانضمام: edsdoj.8ea4b556b83348028b6edeeaaa2e5f33
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:08720169
21831289
DOI:10.32932/pjnh.2021.12.161