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作 者:李宁[1,2] 李维华[1,2] 李州利[1,2] 丁湘[1,2] 范志忠[1,2] 余琦[1,2] 韩永[1,2]
机构地区:[1]解放军第三零九医院 [2]解放军总医院病理科
出 处:《中华外科杂志》1997年第5期294-295,共2页Chinese Journal of Surgery
摘 要:作者报道应用临床病理学、免疫组织化学和电子显微镜检查,发现1例左肾原发性上皮样血管肉瘤伴肾盂移行细胞癌。该病例第八因子相关抗原、荆豆凝集素、内皮细胞抗体、波形蛋白、细胞角蛋白和上皮膜抗原(FⅧRA、UEA、CD31、Vimentin、Cytokeretin和EMA)阳性,电镜查见W-P小体。作者认为该病是一种罕见肿瘤,预后差,其形态学和免疫组织化学类似于上皮性肿瘤,易导致误诊。电镜和内皮性标志物FⅧRA、CD31、UEA的联合应用可确诊本瘤。To understand the clinical characteristics of primary renal epithelioid angiosarcoma.We used clinical pathology,immunohistochemistry and electron microscopy. Analysis and discussion about the case were combined with a review of the literature.We first report a female case of the left renal epithelioid angiosarcoma and concomitantly,transitional cell carcinoma developing from the renal pelvis at age 69.Epithelioid angiosarcoma showed positive results for FⅧRA,UEA,CD 31 ,Cytokeratin and EMA.Weibel Palade bodies were identified by electron microscopy. Primary renal epithelioid angiosarcoma was a rare clinical entity with a poor prognosis,which mimics epithelial tumor,both morphologcally and immunohistochemically,and may be lead to misdiagnosis.The combined use of endothelial cell markers including FⅧRA,CD 31 ,UEA and electronmicroscopy can confirm the diagnosis of this neoplasm.
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