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先天性中线脑穿通畸形的发病机制。

Pathogenesis of congenital midline porencephaly.

作者信息

Stein S C

出版信息

Childs Brain. 1981;8(6):406-16. doi: 10.1159/000120008.

Abstract

A recent report in this journal described 5 children with holoprosencephaly, parietal scalp anomalies and midline intracranial cysts. The authors coined the term 'congenital midline porencephaly' for the clinical syndrome and described the cysts as diverticula of hydrocephalic lateral ventricles. This report describes 3 further children with the same syndrome. The author proposes that the midline cyst is simply a variant of the dorsal cyst reported in other cases of holoprosencephaly. It is further concluded that the cyst arises from primary dysgenesis of cerebral midline structures and is not the result of hydrocephalus. The monoventricle and cyst in these children have the CT scan appearance of the head of a primitive arrow. This 'arrowhead' sign may be helpful in the diagnosis of holoprosencephaly with congenital midline porencephaly.

摘要

该期刊最近的一篇报告描述了5名患有前脑无裂畸形、顶头皮异常和颅内中线囊肿的儿童。作者为该临床综合征创造了“先天性中线孔洞脑畸形”一词,并将囊肿描述为脑积水侧脑室的憩室。本报告描述了另外3名患有相同综合征的儿童。作者提出,中线囊肿仅仅是其他前脑无裂畸形病例中所报道的背侧囊肿的一种变体。进一步得出的结论是,囊肿源于脑中线结构的原发性发育不全,而非脑积水的结果。这些儿童的单脑室和囊肿在CT扫描上呈现出原始箭头头部的外观。这种“箭头征”可能有助于先天性中线孔洞脑畸形型前脑无裂畸形的诊断。

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