Results 71 to 80 of about 7,018 (165)
ABSTRACT Introduction Epithelioid angiomyolipoma is a rare perivascular epithelioid cell tumor subtype with malignant potential. Its morphology mimics renal cell carcinoma, posing diagnostic challenges. Half of these cases harbor TSC1/TSC2 alterations, and a small subset features TFE3 rearrangements, mutually exclusive of TSC mutations.
Yuka Kondo +8 more
wiley +1 more source
HMB45 is a melanoma-specific monoclonal antibody that has found widespread use in diagnostic pathology. Recent reports, however, have suggested that this antibody may cross-react with a small number of carcinomas and other epithelial cells.
SCARPA, Aldo +9 more
core +1 more source
Mucosal Melanoma of Head and Neck: A Rare and Aggressive Disease—A Register‐Based Cohort Study
ABSTRACT Background Mucosal melanomas of the head and neck are rare and often diagnosed in the advanced stage. This study examines the incidence, survival and histology of mucosal melanoma compared to its cutaneous counterpart. Methods This register‐based cohort study reviews head and neck melanomas at Helsinki University Hospital, Finland, from 2002 ...
Sara C. Degerholm +2 more
wiley +1 more source
Amelanotic subungual melanoma (ASM) is a rare variant of nail unit melanoma (NUM) lacking melanin pigmentation, frequently misdiagnosed as a benign post-traumatic or infectious lesion.
Huiru Wang +9 more
doaj +1 more source
Aims To analyse the histo-morphology of cases of medullomyoblastoma and identifying its divergent differentiation. Methods A retrospective review of all cases reported as medulloblastoma between the period of Jan 2000 to Dec 2006 was carried out on ...
Chhabra Rajesh +5 more
doaj +1 more source
L'anticorpo monoclonale correlato ai melanociti HMB45 è caratteristicamente espresso nell'angiomiolipoma ...
M. Pea +10 more
core
Angiomyolipoma with Epithelial Cysts (AMLEC) of the Kidney [PDF]
A 49-year-old man was demonstrated to have two tumors in the right kidney by computed tomographic scan during an examination for cholelithiasis. One was a fat rich solid tumor which was clinically diagnosed as angiomyolipoma, and the other was an ...
武井, 一城 +2 more
core +1 more source
Three mutations in SASH1 cause the pathogenesis of dyschromatosis universalis hereditaria (DUH) [PDF]
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis characterized by hyper- and hypopigmented macules which form a reticulate or mottled pattern.
Zhiyun Wei, Qinghe Xing, Dingan Zhou
core
Background: Immunohistochemical (IHC) stains that distinguish benign, pigmented nail lesions from malignancy are needed. Candidate markers of malignant transformation include p16, HMB45, and Ki-67, with p16 being of particular interest.
Chu, Alex +9 more
core +1 more source
Angiomyolipomes épithélioïdes rénal bénin: à propos de deux cas
Les angiomyolipomes épithélioïdes rénaux (AMLeR) sont des tumeurs rares (identifiées chez moins de 0,1 patients pour 1000 habitants) et représentent 8% des angiomyolipomes (AML) opérés.
Tidiani Bagayogo +5 more
doaj +1 more source

