Suppr超能文献

神经皮肤黑素沉着症伴丹迪-沃克畸形。病例报告及文献复习。

Neurocutaneous melanosis associated with Dandy-Walker malformation. case report and review of the literature.

作者信息

Berker M, Oruckaptan H H, Oge H K, Benli K

机构信息

Neurosurgery Department, Hacettepe University, School of Medicine, Ankara, Turkey.

出版信息

Pediatr Neurosurg. 2000 Nov;33(5):270-273. doi: 10.1159/000055968.

Abstract

Neurocutaneous melanosis is a rare dysmorphogenesis associated with single or multiple giant pigmented cutaneous nevi and diffuse involvement of the leptomeninges anywhere in the central nervous system (CNS). It is interesting that almost 8-10% of patients had associated Dandy-Walker malformation in the literature, suggesting a common origin of the developmental abnormalities. In this article, we present a 2-year-old patient with neurocutaneous melanosis associated with Dandy-Walker malformation. We reviewed the literature and discuss the pathogenesis based on the preferred hypotheses so far.

摘要

神经皮肤黑素沉着症是一种罕见的发育异常,与单个或多个巨大色素性皮肤痣以及中枢神经系统(CNS)任何部位软脑膜的弥漫性受累有关。有趣的是,文献中几乎8%-10%的患者伴有丹迪-沃克畸形,提示发育异常有共同起源。在本文中,我们报告了一名患有神经皮肤黑素沉着症并伴有丹迪-沃克畸形的2岁患者。我们回顾了文献,并根据目前最流行的假说讨论了发病机制。

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