Epithelioid angiomyolipomas:a clinicopathological analysis of 7 cases
10.13315/j.cnki.cjcep.2015.02.011
- VernacularTitle:上皮样血管平滑肌脂肪瘤7例临床病理分析
- Author:
Yuanyuan XU
;
Weiwei HU
;
Liangyun ZHANG
;
Guangmin LI
- Publication Type:Journal Article
- Keywords:
epithelioid angiomyolipoma;
pathology;
immunohistochemistry;
diagnosis
- From:
Chinese Journal of Clinical and Experimental Pathology
2015;(2):161-163,168
- CountryChina
- Language:Chinese
-
Abstract:
Purpose To analyze and summarize morphological characteristics, the immune phenotype, diagnosis and differential diag-nosis, clinical features and prognosis of epithelioid angiomyolipomas retrospectively, to deepen understanding of EAML and improve the diagnostic accuracy. Methods The pathological morphology was observed and immunohistochemistry of phenotypic characteristics were analyzed in 7 cases of epithelioid angiomyolipomas. Results Seven cases of epithelioid angiomyolipomas had similar morphology:larger tumor cells, ovoid, fusiform or polygonal, with abundant and eosinophilic cytoplasm, a big nucleus of different size with obvious nucleoli, polynuclear and gaint tumor cells, with a few mitotic figures. The tumor cells arranged in nests or sheets, cuff-shaped around the blood vessels. Immunohistochemistry showed that the tumor cells were positive for HMB-45, Melan-A, vimentin and SMA, but negative for EMA, CK, and CD10. All of them underwent radical surgery or surgical resection, and were followed up for 3~56 months after operation. 6 cases were alive, without recurrence and metastasis, while 1 case died of gastrointestinal stromal sarcomas 3 months later. Conclusion Epithelioid angiomyolipomas belong to mesenchymal tumors with malignant potential, pathological morphology would be easily misdiagnosed as malignant tumors. Immunohistochemistry plays an important role in the differential diagnosis. Surgical treatment is the main method at present, with possibility of recurrence or metastasis.
