التفاصيل البيبلوغرافية
| العنوان: |
A rapidly growing nodule on the leg of an adolescent: A unique presentation of a non‐neural granular cell tumor. |
| المؤلفون: |
Hobbs, Landon K.1 (AUTHOR) lkh6k@virginia.edu, Kozak, Merrick D.1 (AUTHOR), Gradecki, Sarah E.1 (AUTHOR), McGahren, Eugene D.2 (AUTHOR), Raghavan, Shyam S.1 (AUTHOR) |
| المصدر: |
Journal of Cutaneous Pathology. Dec2022, Vol. 49 Issue 12, p1040-1043. 4p. 3 Color Photographs. |
| مصطلحات موضوعية: |
*CELL tumors, *LYMPHOPROLIFERATIVE disorders, *NEVUS, *ANAPLASTIC lymphoma kinase, *MAST cell disease |
| مستخلص: |
CD68 immunohistochemical stain shows patchy cytoplasmic expression (C, ×400) gl DISCUSSION LeBoit et al first described this tumor in 1991 using the term "primitive polypoid granular cell tumor".[2] Since then, it has been diagnosed in non-polypoid lesions; therefore, the term "non-neural granular cell tumor" has been proposed. 2005; 29 (7): 927 - 934. doi: 10.1097/01.pas.0000157294.55796.d3 4 Chaudhry IH, Calonje E. Dermal non-neural granular cell tumour (so-called primitive polypoid granular cell tumour): a distinctive entity further delineated in a clinicopathological study of 11 cases. Keywords: anaplastic lymphoma kinase; cutaneous neoplasm; dermatopathology; non-neural granular cell tumor; rapidly growing EN anaplastic lymphoma kinase cutaneous neoplasm dermatopathology non-neural granular cell tumor rapidly growing 1040 1043 4 12/01/22 20221201 NES 221201 INTRODUCTION Non-neural granular cell tumor (NNGCT; also known as primitive polypoid GCT) is a rare neoplasm first described by LeBoit et al in 1991 and is considered a diagnosis of exclusion.[[1]] In contrast to classic GCTs, NNGCTs are immunohistochemically distinct, lacking expression of markers of neural differentiation, such as SOX10 and S-100. [Extracted from the article] |
| قاعدة البيانات: |
Academic Search Index |