Suppr超能文献

两例具有毛领征的非典型皮肤膜状发育不全:一例伴真皮黑素细胞增多症,另一例伴鲜红斑痣。

Two cases of atypical membranous aplasia cutis with hair collar sign: one with dermal melanocytosis, and the other with naevus flammeus.

作者信息

Fujita Y, Yokota K, Akiyama M, Machino S, Inokuma D, Arita K, Kimura C, Shimizu H

机构信息

Department of Plastic Surgery, Hakodate Central General Hospital, Hakodate, Japan.

出版信息

Clin Exp Dermatol. 2005 Sep;30(5):497-9. doi: 10.1111/j.1365-2230.2005.01821.x.

Abstract

We report two atypical cases of membranous aplasia cutis surrounded by a rim of hairs, one case associated with dense dermal melanocytosis and the other with naevus flammeus, with characteristic clinical features. A rim of hypertrichosis, 'hair collar' sign, is proposed to have a close association with neuroectodermal defects. A failure of the normal closure of the cranial neural tube might have affected foetal skin development, including melanoblast migration and capillary network formation. The changes in the present cases, as well as the hair collar sign may suggest a complex hamartomatous nature of membranous aplasia cutis.

摘要

我们报告了两例伴有毛发边缘的非典型膜性皮肤发育不全病例,一例与致密性皮肤黑素细胞增多症相关,另一例与鲜红斑痣相关,具有特征性临床特征。提出的一圈多毛症,即“毛领”征,与神经外胚层缺陷密切相关。颅神经管正常闭合失败可能影响胎儿皮肤发育,包括黑素母细胞迁移和毛细血管网络形成。本病例中的变化以及毛领征可能提示膜性皮肤发育不全具有复杂的错构瘤性质。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验