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头皮错构瘤伴异位脑膜上皮成分。一种独特的良性软组织病变,可能类似血管肉瘤。

Hamartoma of the scalp with ectopic meningothelial elements. A distinctive benign soft tissue lesion that may simulate angiosarcoma.

作者信息

Suster S, Rosai J

机构信息

Department of Pathology, Yale University School of Medicine, New Haven, CT 06510-8070.

出版信息

Am J Surg Pathol. 1990 Jan;14(1):1-11. doi: 10.1097/00000478-199001000-00001.

DOI:10.1097/00000478-199001000-00001
PMID:2403758
Abstract

Five cases of a distinctive benign soft tissue lesion of the scalp in patients ranging from 4 months to 40 years of age are described. Clinically, the lesions appeared as solitary, subcutaneous nodules suggestive of a cystic vascular malformation or other benign condition. Histologically, however, the lesions were characterized by a monotonous, pseudoinfiltrative proliferation of cuboidal epithelioid cells arranged in clusters within the dermis and subcutaneous tissue in intimate association with vessels, adipose tissue, and other connective tissue elements. A prominent feature in all cases was the presence of areas simulating freely anastomosing vascular channels lined by round to spindle-shaped, slightly hyperchromatic epithelioid cells reminiscent of angiosarcoma. Immunohistochemically, these cells were negative for factor VIII-related antigen and Ulex europaeus lectin but were strongly positive with vimentin and epithelial membrane antigen antibodies, this latter being in keeping with the immunohistochemical profile of meningothelial cells. The meningothelial nature of these cells was supported by the electron microscopic demonstration in one case of cells with complex, interdigitating cytoplasmic processes that were joined by scattered cell junctions and contained abundant intracytoplasmic intermediate filaments. The intimate admixture of meningothelial elements with haphazardly arranged connective tissue elements sets these lesions apart from cutaneous meningiomas and warrants their designation as hamartomas with an ectopic meningothelial component.

摘要

本文描述了5例头皮独特的良性软组织病变患者,年龄从4个月至40岁不等。临床上,病变表现为孤立的皮下结节,提示为囊性血管畸形或其他良性病变。然而,组织学上,病变的特征是立方形上皮样细胞呈单调的假浸润性增生,这些细胞在真皮和皮下组织内聚集成簇,与血管、脂肪组织和其他结缔组织成分密切相关。所有病例的一个突出特征是存在模拟自由吻合血管通道的区域,这些通道内衬圆形至梭形、轻度深染的上皮样细胞,让人联想到血管肉瘤。免疫组织化学显示,这些细胞对VIII因子相关抗原和欧洲荆豆凝集素呈阴性,但对波形蛋白和上皮膜抗原抗体呈强阳性,后者与脑膜内皮细胞的免疫组织化学特征相符。在一例病例中,电子显微镜显示细胞具有复杂的、相互交错的胞质突起,这些突起通过散在的细胞连接相连,并含有丰富的胞质中间丝,支持了这些细胞的脑膜内皮性质。脑膜内皮成分与随意排列的结缔组织成分的紧密混合使这些病变有别于皮肤脑膜瘤,因此将其命名为具有异位脑膜内皮成分的错构瘤。

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