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婴儿期软脑膜瘘管:两例报告及文献综述,特别关注破裂组

Pial fistula in infancy: Report of two cases and literature review with special emphasis on the ruptured group.

作者信息

Mahmoud Mostafa, Abdalla Ramez Nader, Mohamed Ayman Hemdan, Farid Mostafa

机构信息

1 Ain Shams University, Interventional Neuroradiology Unit/Radiology Department, Cairo, Egypt.

2 Dr Soliman Fakeeh Hospital, Interventional Neuroradiology Unit/Radiology Department, Jeddah, Makkah, Saudi Arabia.

出版信息

Interv Neuroradiol. 2018 Aug;24(4):444-449. doi: 10.1177/1591019918763146. Epub 2018 Mar 21.

Abstract

Cerebral pial fistula is a rare vascular pathology with no more than 150 cases reported. Most cases reported in infancy have been published as case reports. Owing to its high flow, its occurrence in this age group carries the potential risk of heart failure, chronic venous hypertension, seizures and, less frequently, cerebral haemorrhage. We present two cases of pial fistulae in infancy treated by endovascular embolisation using N-butyl cyanoacrylate. A review of the English-language literature was performed for this age group with special emphasis on ruptured cases.

摘要

脑软膜瘘是一种罕见的血管病变,报告的病例不超过150例。大多数在婴儿期报告的病例都作为病例报告发表。由于其高流量,在这个年龄组中发生会有心力衰竭、慢性静脉高压、癫痫发作的潜在风险,较少见的还有脑出血。我们介绍两例婴儿期软膜瘘病例,采用氰基丙烯酸正丁酯进行血管内栓塞治疗。针对这个年龄组进行了英文文献综述,特别强调破裂病例。

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Congenital pial arteriovenous fistula in the temporal region draining into cavernous sinus: a case report.
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