Tai Yanhong, Wei Lixin, Shi Huaiyin
Department of Pathology, General Hospital of the People's Liberation Army, Beijing, China.
Pediatr Dev Pathol. 2010 Sep-Oct;13(5):412-4. doi: 10.2350/09-10-0726-CR.1. Epub 2010 Jan 19.
We report a case of cardiac perivascular epithelioid cell tumor (PEComa) that occurred in a 10-year-old girl. The patient presented with cardiac murmur and increasing dyspnea. A solid mass was detected in the left atrioventricular groove by sonography and chest computed tomography. Histologic examination revealed a tumor composed of spindle and epithelioid cells, exhibiting either a clear or a slightly eosinophilic cytoplasm and a bland nucleus. Intranuclear pseudoinclusions and calcifications could be found occasionally. Immunohistochemically, tumor cells were positive for HMB45, melan-A, and smooth muscle actin. We regard this case as a PEComa of uncertain malignant potential. The patient remains disease free at her 18-month follow up. To the best of our knowledge, this is the 3rd report of cardiac PEComa and the 1st report of cardiac PEComa affecting a child.
我们报告了一例发生在一名10岁女孩身上的心脏血管周上皮样细胞瘤(PEComa)。患者表现为心脏杂音和进行性呼吸困难。超声心动图和胸部计算机断层扫描在左房室沟发现一个实性肿块。组织学检查显示肿瘤由梭形细胞和上皮样细胞组成,细胞质呈透明或轻度嗜酸性,细胞核温和。偶尔可见核内假包涵体和钙化。免疫组织化学检查显示,肿瘤细胞HMB45、黑色素A和平滑肌肌动蛋白呈阳性。我们认为该病例为恶性潜能不确定的PEComa。患者在18个月的随访中无疾病复发。据我们所知,这是心脏PEComa的第3例报告,也是影响儿童的心脏PEComa的首例报告。