A 10-year-old girl with coexistent Moyamoya disease and Graves' disease

被引：16
作者：
Golomb, MR
Biller, J
Smith, JL
Edwards-Brown, M
Sanchez, JC
Nebesto, TD
Garg, BP
机构：
[1] Riley Hosp, Div Pediat Neurol, Dept Neurol, Indianapolis, IN 46202 USA
[2] Riley Hosp, Indiana Univ Sch Med, Indianapolis, IN USA
[3] Loyola Univ, Dept Neurol, Med Ctr, Stritch Sch Med, Chicago, IL USA
[4] Indiana Univ, Sch Med, Dept Neurosurg, Riley Hosp, Indianapolis, IN USA
[5] Indiana Univ, Sch Med, Dept Neuroradiol, Riley Hosp, Indianapolis, IN USA
[6] Indiana Univ, Sch Med, Sect Pediat endocrinol, Eiley Hosp, Indianapolis, IN USA
[7] Indiana Univ, Sch Med, Div Pediat Neurol, Riley Hosp, Indianapolis, IN USA
来源：
JOURNAL OF CHILD NEUROLOGY | 2005年 / 20卷 / 07期
关键词：
D O I：
10.1177/08830738050200071801
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
There are rare reports of young women with moyamoya, disease associated with Graves' disease; we are unaware of any previous reports of this association in prepubescent girls. We report a 10-year-old girl who presented with multiple bilateral strokes. Cerebral angiography demonstrated moderate to severe stenosis of her bilateral distal internal carotid arteries and proximal anterior and middle cerebral arteries, which was greater on the right. Thyroid function tests demonstrated suppressed thyroid-stimulating hormone and elevated thyroid hormone levels. Serum antiphospholipid antibody screen demonstrated mild elevations of antiocardiolipin IgG. Possible mechanisms predisposing individuals to concurrent moyamoya and Graves' disease are discussed.
引用
收藏
页码：620 / 624
页数：5
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