内蒙古医科大学学报
內矇古醫科大學學報
내몽고의과대학학보
Journal of Inner Mongolia Medical University
2015年
2期
117-121
,共5页
郭彦%宋晓燕%周青波%都吉雅%汪锋%朱淑芬
郭彥%宋曉燕%週青波%都吉雅%汪鋒%硃淑芬
곽언%송효연%주청파%도길아%왕봉%주숙분
肾集合管癌%临床病理%电镜%免疫组化
腎集閤管癌%臨床病理%電鏡%免疫組化
신집합관암%림상병리%전경%면역조화
collecting duct carcinoma of the kidney%clinical pathology%electron microscope%im-munohistochemistry
目的::探讨罕见的肾集合管癌( collecting duct carcinoma,CDC)的临床病理特征、诊断及鉴别诊断。方法:对5例 CDC 进行临床病理学和电镜观察及免疫组化标记,并复习相关文献。结果:肿瘤细胞呈腺管状、乳头状及条索状排列,伴间质纤维化和炎症细胞反应,肿瘤旁集合管上皮细胞可见异型增生;免疫表型示肿瘤细胞CKpan、CK 7、CK 19、PAX 8、EMA均(+),vimentin部分(+)(2/5),CK 20、CD 10、P 63、Villin均(-)。电镜观察肿瘤细胞胞浆较丰富,细胞腔面见少量发育不好的短小微绒毛,可见发育不好的细胞连接。结论:CDC是一种高度恶性的肾上皮性肿瘤,较罕见,易误诊,诊断时应与乳头状肾细胞癌、腺样结构的尿路上皮癌、肾髓质癌及转移性腺癌等鉴别,免疫组化及电镜有助于诊断及鉴别诊断。
目的::探討罕見的腎集閤管癌( collecting duct carcinoma,CDC)的臨床病理特徵、診斷及鑒彆診斷。方法:對5例 CDC 進行臨床病理學和電鏡觀察及免疫組化標記,併複習相關文獻。結果:腫瘤細胞呈腺管狀、乳頭狀及條索狀排列,伴間質纖維化和炎癥細胞反應,腫瘤徬集閤管上皮細胞可見異型增生;免疫錶型示腫瘤細胞CKpan、CK 7、CK 19、PAX 8、EMA均(+),vimentin部分(+)(2/5),CK 20、CD 10、P 63、Villin均(-)。電鏡觀察腫瘤細胞胞漿較豐富,細胞腔麵見少量髮育不好的短小微絨毛,可見髮育不好的細胞連接。結論:CDC是一種高度噁性的腎上皮性腫瘤,較罕見,易誤診,診斷時應與乳頭狀腎細胞癌、腺樣結構的尿路上皮癌、腎髓質癌及轉移性腺癌等鑒彆,免疫組化及電鏡有助于診斷及鑒彆診斷。
목적::탐토한견적신집합관암( collecting duct carcinoma,CDC)적림상병리특정、진단급감별진단。방법:대5례 CDC 진행림상병이학화전경관찰급면역조화표기,병복습상관문헌。결과:종류세포정선관상、유두상급조색상배렬,반간질섬유화화염증세포반응,종류방집합관상피세포가견이형증생;면역표형시종류세포CKpan、CK 7、CK 19、PAX 8、EMA균(+),vimentin부분(+)(2/5),CK 20、CD 10、P 63、Villin균(-)。전경관찰종류세포포장교봉부,세포강면견소량발육불호적단소미융모,가견발육불호적세포련접。결론:CDC시일충고도악성적신상피성종류,교한견,역오진,진단시응여유두상신세포암、선양결구적뇨로상피암、신수질암급전이성선암등감별,면역조화급전경유조우진단급감별진단。
Objective:To investigate the collecting duct carcinoma of the kidney ( collecting duct rare carcinoma, CDC ) in diagnosis and differential diagnosis of clinical and pathological features. Methods:clinical pathology and electron microscope and immunohistochemistry was performed on 5 patients with CDC,and review of the literature. Results:the tumor cells were tubular,papillary and cord like arrangements, with interstitial fibrosis and inflammatory cell reaction, tumor adjacent to the collecting duct epithelial cells were atypical;immunophenotyping showed the tumor cells CKpan,CK 7, CK 19,PAX 8,EMA were(+),part vimentin(+),CK 20(2/5),CD 10,P 63,Villin(-). Electron mi-croscope observation of tumor cell cytoplasm is rich,lumen meet a few bad development of short and small microvilli,visible bad development of cellular connection. Conclusion:CDC is a highly malignant renal epithelial tumors, are rare, misdiagnosis, diagnosis should be differentiated with papillary renal cell carcinoma,adenoid structure of urothelial carcinoma,renal medullary carcinoma and metastatic ad-enocarcinoma,immunohistochemistry and electron microscopy is helpful in the diagnosis and differential diagnosis.