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软骨发育不全与Chiari II型畸形并存:延髓颈髓交界处的双重打击。

Concomitant achondroplasia and Chiari II malformation: A double-hit at the cervicomedullary junction.

作者信息

Awad Al-Wala, Aleck Kyrieckos A, Bhardwaj Ratan D

机构信息

Al-Wala Awad, College of Medicine-Phoenix, University of Arizona, Phoenix, AZ 85004, United States.

出版信息

World J Clin Cases. 2014 Nov 16;2(11):711-6. doi: 10.12998/wjcc.v2.i11.711.

Abstract

We report the first case of a neonate with concurrent Chiari II malformation and achondroplasia. Although rare, both these conditions contribute to several deleterious anatomical changes at the cervicomedullary junction and thus predispose to acute hydrocephalus. Although our patient was initially asymptomatic, hydrocephalus ensued several weeks after birth and required cerebral spinal fluid diversion. We discuss the potential links between the two conditions, the pathophysiology, and the important clinical implications for the management of the increased risk of hydrocephalus.

摘要

我们报告了首例同时患有Chiari II型畸形和软骨发育不全的新生儿病例。尽管这两种情况都很罕见,但它们都会导致颈髓交界处出现一些有害的解剖学变化,从而易引发急性脑积水。尽管我们的患者最初没有症状,但出生几周后出现了脑积水,需要进行脑脊液分流。我们讨论了这两种情况之间的潜在联系、病理生理学以及对于管理脑积水风险增加的重要临床意义。

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本文引用的文献

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