Dimmler A, Seitz G, Hohenberger W, Kirchner T, Faller G
Institute of Pathology, University of Erlangen-Nuremberg, Krankenhausstrasse 8-10, 91054 Erlangen, Germany.
J Clin Pathol. 2003 Aug;56(8):627-8. doi: 10.1136/jcp.56.8.627.
Perivascular epithelioid cell tumours (PEComas) other than angiomyolipoma, clear cell "sugar" tumour of the lung, and lymphangioleiomyomatosis are very rare mesenchymal tumours. The uterus seems to be the most prevalent site of involvement, but only 13 cases of uterine PEComa have been described. Three of these cases exhibited local aggressive behaviour and only one showed metastasis. Because of the extremely small number of cases, PEComas are considered tumours of uncertain malignant potential. This report describes a 68 year old woman, who presented with multiple pulmonary lesions seven years after the initial diagnosis of well differentiated endometrial stromal sarcoma. Histological and immunohistochemical analysis of the pulmonary lesions, in addition to re-evaluation of the primary uterine tumour, led to the final diagnosis of metastatic uterine PEComa. The findings indicate that any PEComa might have malignant potential. Spreading of this tumour to other organs might become evident even several years after primary manifestation.
除血管平滑肌脂肪瘤、肺透明细胞“糖”瘤和淋巴管平滑肌瘤病外,血管周上皮样细胞瘤(PEComas)是非常罕见的间叶组织肿瘤。子宫似乎是最常受累的部位,但仅有13例子宫PEComa的病例报道。其中3例表现出局部侵袭性,仅有1例发生转移。由于病例数量极少,PEComas被认为是恶性潜能不确定的肿瘤。本报告描述了一名68岁女性,在最初诊断为高分化子宫内膜间质肉瘤7年后出现多发肺部病变。对肺部病变进行组织学和免疫组化分析,并对原发性子宫肿瘤进行重新评估后,最终诊断为转移性子宫PEComa。这些发现表明,任何PEComa都可能具有恶性潜能。即使在原发表现出现数年之后,这种肿瘤向其他器官的扩散也可能变得明显。