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先天性局限性多毛症伴发的皮肤脑膜瘤。

Cutaneous meningioma underlying congenital localized hypertrichosis.

作者信息

Peñas P F, Jones-Caballero M, Amigo A, Aragüés M, García-Diéz A

机构信息

Department of Dermatology, Hospital de la Princesa, Universidad Autónoma, Madrid, Spain.

出版信息

J Am Acad Dermatol. 1994 Feb;30(2 Pt 2):363-6. doi: 10.1016/s0190-9622(94)70041-9.

Abstract

A 28-year-old man had a circumscribed hypertrichotic area on the left lumbar region since birth. A biopsy specimen showed numerous normal-appearing hair follicles and arrector pili muscles. In the subcutaneous layer a mass of dense collagenous connective tissue formed the background in which ill-defined foci of meningothelial cells in nests and pseudovascular spaces were seen. Collagenous structures (pseudopsammoma bodies), some of which showed calcification (psammoma bodies), were also seen. A diagnosis of cutaneous meningioma was made.

摘要

一名28岁男性自出生以来左腰区有一局限性多毛区域。活检标本显示有许多外观正常的毛囊和立毛肌。在皮下层,一团致密的胶原结缔组织构成背景,其中可见巢状和假血管间隙内界限不清的脑膜上皮细胞灶。还可见到胶原结构(假砂粒体),其中一些显示钙化(砂粒体)。诊断为皮肤脑膜瘤。

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