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脑裂畸形,发育性血管病变的后果?一份临床病理报告。

Schizencephaly, consequence of a developmental vasculopathy? A clinicopathological report.

作者信息

Landrieu P, Lacroix C

机构信息

Department of Pediatric Neurology, CHU Bicêtre, France.

出版信息

Clin Neuropathol. 1994 Jul-Aug;13(4):192-6.

PMID:7955664
Abstract

Schizencephaly was diagnosed by CT scan in a 3-month-old girl who died soon thereafter. The main neuropathological findings were the following: 1) A left frontal and a right parietal cleft were present which consisted in mesenchymal spaces taking the place of localized developmental defects of the cerebral mantel. 2) The gray matter lining the clefts was a microgyric cortical ribbon deeply infolded in the hemisphere without evidence of arrested neuronal migration. 3) However, true subependymal heterotopia were also recorded in areas distant from the microgyric ribbon. It is suggested that schizencephaly is initiated before the end of neuronal migration, at a time when the full thickness of the cerebral mantel can be easily destroyed by a localized malacic process, not later than 20 weeks of gestation. 4) Late ischemic insults to the cerebral cortex were observed, suggesting a long lasting process. Moreover, the death was due to an hematoma in the largest cleft, where atypical vessels were present. A developmental vasculopathy could be the cause for some cases of schizencephaly and could be life-threatening until the postnatal life.

摘要

一名3个月大的女孩经CT扫描诊断为脑裂畸形,随后不久死亡。主要神经病理学发现如下:1)存在左侧额叶和右侧顶叶裂隙,由间充质间隙组成,取代了脑皮质局部发育缺陷的位置。2)裂隙内衬的灰质是一条微脑回皮质带,深深折叠在半球内,无神经元迁移停滞的证据。3)然而,在远离微脑回带的区域也记录到了真正的室管膜下异位。提示脑裂畸形在神经元迁移结束前开始,此时脑皮质全层可因局部软化过程而轻易被破坏,不晚于妊娠20周。4)观察到大脑皮质晚期缺血性损伤,提示这是一个持续较长时间的过程。此外,死亡原因是最大裂隙内的血肿,其中存在非典型血管。发育性血管病变可能是某些脑裂畸形病例的病因,并且在出生后可能危及生命。

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