一个非常罕见的病例报告晚提出莫亚莫亚综合征的儿童结核性脑膜炎的历史

K. Umesh, K. Shilpa
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引用次数: 0

摘要

莫亚病是一种罕见的特发性进行性血管闭塞性疾病,其特征是进入颅骨的通往大脑的主要血管不可逆转地闭塞。闭塞过程刺激基底、经皮质和经硬膜侧支血管扩大的广泛网络的发展,阻塞容易引起中风或癫痫发作。脑血管狭窄的过程似乎是脑血管对各种外部刺激、损伤或遗传缺陷的反应。我们提出了一例进行性血管病变的10岁女孩与结核性脑膜炎的历史,在婴儿期,这是很少被描述在儿童人口中结核性脑膜炎仍然是非常常见的在这个部分的世界。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A very rare case report of late presentation of Moya moya syndrome in a child with history of tubercular meningitis
Moya Moya is a rare idiopathic progressive vaso-occlusive disease characterized by irreversible occlusion of main blood vessels to the brain as they enter into the skull. The occlusive process stimulates the development of an extensive network of enlarged basal, transcortical and transdural collateral vessels The blockage tends to cause strokes or seizures. The process of narrowing of cerebral vessels seems to be a reaction of brain blood vessels to a wide variety of external stimuli, injuries or genetic defects.We present a case of progressive vasculopathy in a 10 year old girl with history of tubercular meningitis in the infancy and which is being rarely described in pediatric population in which tubercular meningitis is still very much common in this part of world.
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