Sukov William R, Cheville John C, Amin Mahul B, Gupta Ruta, Folpe Andrew L
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Am J Surg Pathol. 2009 Feb;33(2):304-8. doi: 10.1097/PAS.0b013e3181854929.
The perivascular epithelioid cell family of tumors (PEComas) includes familiar lesions such as angiomyolipoma, lymphangioleiomyoma, and clear-cell "sugar" tumors of the lung. Less frequently, PEComas arise in various other locations throughout the body including soft tissue, bone, and visceral organs. We report 3 cases of PEComa arising in the urinary bladder in 2 men in their fourth decade, and 1 woman in her third decade. All 3 tumors showed histologic features characteristic of PEComa including spindled and epithelioid cell morphology with variable clear cell change, and all coexpressed melanocytic and smooth muscle associated markers by immunohistochemistry. Follow-up demonstrated an indolent course for 2 patients with no evidence of disease at 10 and 21 months, respectively, and the third case was recently diagnosed. We also provide a review of the 4 previously reported PEComas occurring in the bladder. PEComas of the urinary bladder should be carefully distinguished from a variety of histologically similar, but clinically dissimilar entities.
血管周上皮样细胞瘤(PEComas)家族包括一些常见病变,如血管平滑肌脂肪瘤、淋巴管平滑肌瘤和肺透明细胞“糖”瘤。较少见的是,PEComas发生于身体其他各个部位,包括软组织、骨骼和内脏器官。我们报告了3例膀胱PEComas,其中2例为40岁左右的男性,1例为30岁左右的女性。所有3例肿瘤均表现出PEComas的组织学特征,包括梭形和上皮样细胞形态以及不同程度的透明细胞改变,并且通过免疫组织化学均共表达黑素细胞和平滑肌相关标志物。随访显示,2例患者病情进展缓慢,分别在10个月和21个月时无疾病证据,第三例患者最近被诊断。我们还对先前报道的4例膀胱PEComas进行了综述。膀胱PEComas应与多种组织学相似但临床不同的实体仔细区分。