成年伴高位基底动脉的先天性导水管狭窄的晚期表现:1例报告。

IF 0.6 Q4 CLINICAL NEUROLOGY
Journal of Neurological Surgery Reports Pub Date : 2025-01-20 eCollection Date: 2025-01-01 DOI:10.1055/s-0044-1788037
Hassan Mohammed Alturiki, Batool M Alqudihi, Shima Alboesa, Abdullah H Alramadan
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引用次数: 0

摘要

背景先天性输水管狭窄(CAS)是一种罕见的变异,被称为成人发病的CAS,其特征是在成年期出现症状。病例描述一名35岁男性主诉急性头痛和呕吐。脑磁共振成像显示急性脑积水由于输水管网。病人接受脑室腹腔分流术治疗,情况良好。他的病情因过度分流而并发硬膜下血肿,通过额顶骨开颅治疗,最终他接受了可编程瓣膜翻修。结论成人导水管狭窄的假说有待进一步研究。这将有助于阐明无症状儿童期,并通过早期识别晚期CAS,潜在地减少并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late Presentation of Congenital Aqueduct Stenosis in Adulthood with High-Riding Basilar Artery: Case Report.

Background  A rare variant of congenital aqueductal stenosis (CAS) is known as adult-onset CAS, characterized by the emergence of symptoms during adulthood. Case Description  A 35-year-old man presented complaining of acute-onset headache and vomiting. Magnetic resonance imaging of the brain revealed an acute hydrocephalus due to an aqueductal web. The patient was treated with a ventriculoperitoneal shunt and doing well. His condition was complicated by subdural hematoma as a result of overshunting, which was treated by frontoparietal craniotomy and eventually, he underwent valve revision to a programmable valve. Conclusion  Additional research is needed to gain a deeper understanding of the hypothesis related to adult aqueductal stenosis. This will help shed light on the asymptomatic childhood phase and potentially reduce complications by identifying late CAS early.

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