Suppr超能文献

[先天性皮肤发育不全患者的大面积头皮和颅骨缺损]

[Large scalp and skull defect in patient with aplasia cutis congenita].

作者信息

Henriques José Gilberto de Brito, Pianetti Filho Geraldo, Giannetti Alexandre Varella, Henriques Karina Santos Wandeck

机构信息

Hospital das Clínicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Arq Neuropsiquiatr. 2004 Dec;62(4):1108-11. doi: 10.1590/s0004-282x2004000600034. Epub 2004 Dec 15.

Abstract

Aplasia cutis congenita is a rare condition characterized by the absence of skin layers. It is most common on the scalp, middle line, and it can be seen as a congenital ulcer involving periosteum, skull and dura. We present the case of a female newborn infant with a dysmorphic facies, a large scalp and skull defect exposing the dura. There was no cerebrospinal fluid leakage. The rarity of cases with large defects and small series reported make difficult to determinate the ideal treatment for aplasia cutis congenita. More studies are necessary to define the etiology and best management of this patients.

摘要

先天性皮肤发育不全是一种罕见的疾病,其特征是皮肤层缺失。它最常见于头皮中线,可表现为累及骨膜、颅骨和硬脑膜的先天性溃疡。我们报告了一例患有面部畸形、巨大头皮和颅骨缺损并暴露硬脑膜的女性新生儿病例。没有脑脊液漏。由于大缺损病例罕见且报道的病例系列较少,难以确定先天性皮肤发育不全的理想治疗方法。需要更多研究来明确该疾病的病因和最佳治疗方案。

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