Luo Dong-lan, Liu Yan-hui, Zhuang Heng-guo, Luo Xin-lan
Department of Pathology and Medical Laboratory, Guangdong Provincial People's Hospital, Guangzhou 510080, China.
Zhonghua Yi Xue Za Zhi. 2007 Nov 6;87(41):2909-13.
To investigate the clinicopathologic features of tumors showing perivascular epithelioid cell differentiation (PEComas).
The clinicopathologic data of 39 cases pf angiomyolipoma (AML), 17 males and 22 females, with the primary focus in the kidney on 30 cases, in the liver in 4 cases, in the lung, uterus and broad ligament, abdominal wall, retroperitoneum, and nasal cavity in 1 case respectively, were analyzed. Immunohistochemistry (HIC) was used to detect the expression of pan-cytokeratin (CK), S-100 protein, smooth muscle actin (SMA), desmin, vimentin, HMB45, Melan-A, microphthalmia transcription factor (MiTF), CD117, and CD34 in the specimens of the tumors obtained during operation. Twenty patients were followed up.
Pathological examination showed branched capillaries or arterioles, often thick-walled similar to those in the renal cell carcinoma, and the cancerous cells consisting of the mixture of epithelial cells and spindle cells. HIC showed that the expression rates of Melan-A, HMB45, MITF, SMA, desmin, S-100 protein, vimentin, CD117, CK, and CD34 were 95% (37/39), 72% (32/39), 46% (18/39), 82% (32/39), 27% (10/39), 15% (6/39), 82% (32/39), 10% (4/39), 0, and 0 respectively. Clinical follow-up showed 1 patient alive with tumor, and 19 alive free from disease.
PEComas have distinctive morphological and immunohistochemical features.
探讨具有血管周上皮样细胞分化(PEComas)的肿瘤的临床病理特征。
分析39例血管平滑肌脂肪瘤(AML)的临床病理资料,其中男性17例,女性22例,30例原发灶位于肾脏,4例位于肝脏,1例分别位于肺、子宫、阔韧带、腹壁、腹膜后和鼻腔。采用免疫组织化学(HIC)检测手术切除肿瘤标本中泛细胞角蛋白(CK)、S-100蛋白、平滑肌肌动蛋白(SMA)、结蛋白、波形蛋白、HMB45、Melan-A、小眼转录因子(MiTF)、CD117和CD34的表达。对20例患者进行了随访。
病理检查显示分支状毛细血管或小动脉,壁常增厚,类似于肾细胞癌,癌细胞由上皮细胞和梭形细胞混合组成。HIC显示Melan-A、HMB45、MITF、SMA、结蛋白、S-100蛋白、波形蛋白、CD117、CK和CD34的表达率分别为95%(37/39)、72%(32/39)、46%(18/39)、82%(32/39)、27%(10/39)、15%(6/39)、82%(32/39)、10%(4/39)、0和0。临床随访显示1例患者带瘤生存,19例无病生存。
PEComas具有独特的形态学和免疫组织化学特征。