Sun Ke, Zhao Ming, Yao Hongtian, Wang Lijun, Wei Jianfeng
Department of Pathology, The First Affiliated Hospital, Zhengjiang University Medicine School Hangzhou 310003, Zhejiang, P. R. China.
Department of Pathology, Zhejiang Provincial People's Hospital Hangzhou 310014, Zhejiang, P. R. China.
Int J Clin Exp Pathol. 2014 Oct 15;7(11):8170-5. eCollection 2014.
We report the first case of inflammatory variant of hepatic angiomyolipoma (AML) with expression of transcription factor E3 (TFE3) protein but negativity for HMB45 and melan A in a 62-year-old female. Imaging studies revealed a tumor in the left lobe of liver, sized 5.8 cm in maximum diameter. Microscopically, the lesion was composed of large polygonal or epithelioid cells with copious eosinophilic granular cytoplasm. There was a very prominent stromal lymphoplasmacytic infiltrate. Immunohistochemically, the tumor cells showed very strong and diffuse positivity for smooth muscle actin, and cathepsin K, while S-100 protein, keratin, desmin, HMB45 and Melan-A are negative. However, there was multifocal and very convincing nuclear positivity for TFE3, thus confirms the diagnosis.
我们报告了首例肝血管平滑肌脂肪瘤(AML)炎症变体病例,该病例为一名62岁女性,其转录因子E3(TFE3)蛋白呈阳性表达,但HMB45和黑素A呈阴性。影像学检查显示肝脏左叶有一个肿瘤,最大直径为5.8厘米。显微镜下,病变由具有丰富嗜酸性颗粒细胞质的大的多边形或上皮样细胞组成。有非常明显的间质淋巴细胞和浆细胞浸润。免疫组织化学显示,肿瘤细胞对平滑肌肌动蛋白和组织蛋白酶K呈非常强烈且弥漫性阳性,而S-100蛋白、角蛋白、结蛋白、HMB45和黑素A均为阴性。然而,TFE3呈多灶性且非常令人信服的核阳性,从而确诊。