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Perivascular Epithelioid Cell Tumor of Urinary Bladder.

Authors :
Wu, You-li
Lang, Lang
Ma, Qiang
Wu, Feng
Zhang, Yu
Chen, Wei
Yan, Xiao-chu
Duan, Guang-jie
Source :
American Journal of Clinical Pathology. Jul2021, Vol. 156 Issue 1, p56-71. 16p.
Publication Year :
2021

Abstract

<bold>Objectives: </bold>To review the clinicopathologic features of perivascular epithelioid cell tumor (PEComa) of the urinary bladder.<bold>Methods: </bold>Seven cases of bladder PEComa were studied by light microscopy, immunohistochemistry, and fluorescence in situ hybridization (FISH).<bold>Results: </bold>In our 7 cases, 5 patients were female and 2 were male, with ages between 26 and 78 years. Patients presented with hematuria and recurrent abdominal discomfort as the main clinical symptoms. Microscopically, the epithelioid and spindle-shaped tumor cells with clear to granular eosinophilic cytoplasm were arranged in fascicular, acinar, or nested patterns. The tumor cells were positive for HMB45, melan-A, and SMA, but no TFE3 gene rearrangement was detected in any of the 7 samples by FISH. The analysis of all 35 cases from the literature and ours showed a patient age range from 16 to 78 years (mean age, 39 years), a male-to-female ratio of 1:1.3, maximal tumor diameters from 0.6 to 18.8 cm (mean, 4.5 cm). With a mean follow-up of 27 months, the recurrence, metastasis, and mortality rates were 10.7%, 10.7%, and 7.1%, respectively.<bold>Conclusions: </bold>Bladder PEComa is extremely rare, remains a diagnostic challenge, and needs more attention. Strengthening the understanding of this tumor will improve diagnostic accuracy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029173
Volume :
156
Issue :
1
Database :
Academic Search Index
Journal :
American Journal of Clinical Pathology
Publication Type :
Academic Journal
Accession number :
151010708
Full Text :
https://doi.org/10.1093/ajcp/aqaa204