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血管周上皮样细胞肿瘤(PEComas):4例恶性病例扩展了组织病理学谱并描述了一项独特发现。

Perivascular epithelioid cell neoplasms (PEComas): four malignant cases expanding the histopathological spectrum and a description of a unique finding.

作者信息

Weinreb Ilan, Howarth David, Latta Eleanor, Ghazarian Danny, Chetty Runjan

机构信息

Department of Pathology, University Health Network, 200 Elizabeth Street, 11th Floor, Toronto, ON, M5G 2C4, Canada.

出版信息

Virchows Arch. 2007 Apr;450(4):463-70. doi: 10.1007/s00428-007-0378-7. Epub 2007 Feb 15.

Abstract

Four cases of malignant PEComas were stained with smooth muscle actin, muscle specific actin, desmin, human melanoma black-45, melan-A, microphthalmia transcription factor, S100 and cyclin D1. One case was studied by electron microscopy (EM). Tumour locations were the thigh, elbow, retroperitoneum and bladder in association with a urachal cyst. There were two men and two women; the average age was 51.3 years, and the size ranged from 5.0-23.0 cm. In three cases, 50-95% of the tumour was composed of pleomorphic sarcomatous areas. All cases had at least focal clear-cell areas. One case showed a continuous single layer of perivascular clear cells remote from the tumour, transitioning to invasive nests and to PEComa. EM demonstrated these cells in apposition to and in direct contact with the abluminal surface of the basal lamina of the capillaries. We suggest the term "pecosis" for these areas. All cases were positive for two or more melanocytic markers and for at least one actin. S100 and desmin were focally positive in one case. Cyclin D1 was positive in 3:4 cases. Four cases of malignant PEComa are described with the existence of a unique lesion (pecosis) in one case. These tumours may manifest largely as sarcomas appearing to be undifferentiated and should be considered in their differential diagnosis.

摘要

对4例恶性PEComa进行平滑肌肌动蛋白、肌特异性肌动蛋白、结蛋白、人黑素瘤黑色素-45、黑素A、小眼畸形转录因子、S100和细胞周期蛋白D1染色。1例进行了电子显微镜(EM)研究。肿瘤部位分别为大腿、肘部、腹膜后和膀胱伴脐尿管囊肿。患者为2男2女;平均年龄51.3岁,大小范围为5.0 - 23.0 cm。3例中,50 - 95%的肿瘤由多形性肉瘤样区域组成。所有病例均至少有局灶性透明细胞区域。1例显示远离肿瘤的连续单层血管周围透明细胞,过渡为浸润性巢状结构和PEComa。EM显示这些细胞与毛细血管基膜的管腔外表面相邻并直接接触。我们建议将这些区域称为“pecosis”。所有病例两种或更多黑素细胞标记物阳性,且至少一种肌动蛋白阳性。1例中S100和结蛋白局灶性阳性。细胞周期蛋白D1在4例中有3例阳性。描述了4例恶性PEComa,其中1例存在独特病变(pecosis)。这些肿瘤可能主要表现为未分化的肉瘤,在鉴别诊断中应予以考虑。

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