Moyamoya Disease Associated With Hereditary Spherocytosis

被引：9

作者：

Van, Philippe Vo ^{[1
]}

Sabouraud, Pascal ^{[1
]}

Mac, Gratiela ^{[2
]}

Abely, Michel ^{[1
]}

Bednarek, Nathalie ^{[1
]}

机构：

[1] Univ Hosp Ctr Reims, Dept Pediat, F-51092 Reims, France

[2] Univ Hosp Ctr Reims, Dept Radiol, F-51092 Reims, France

来源：

PEDIATRIC NEUROLOGY | 2011年 / 44卷 / 01期

关键词：

D O I：

10.1016/j.pediatrneurol.2010.08.002

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

A 5-year-old girl with hereditary spherocytosis presented with two episodes of transient ischemic attacks within a month. Cranial magnetic resonance imaging angiography revealed a left internal carotid artery and middle cerebral artery stenosis, with an extensive vascular mesh in the thalamic area indicative of moyamoya disease. Treatment consisted of supporting cerebral perfusion with blood transfusions, and splenectomy to prevent recurrence. Moyamoya disease is a very unusual cerebrovascular disorder in childhood and its association with hereditary spherocytosis is rarely reported. (C) 2011 by Elsevier Inc. All rights reserved.

引用

页码：69 / 71

页数：3

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