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多发性动静脉畸形伴独立病灶,病例报告及文献复习

Multiple AVM with separate nidi, a case report and review the literatures.

作者信息

Taheri Morteza, Rahmatian Aryoobarzan, Javadnia Parisa

机构信息

Department of Neurosurgery, Iran University of Medical Sciences, Tehran, Iran.

Department of Neurosurgery, Ilam University of Medical Sciences, Ilam, Iran.

出版信息

J Cerebrovasc Endovasc Neurosurg. 2024 Dec;26(4):412-417. doi: 10.7461/jcen.2024.E2024.05.002. Epub 2024 Oct 10.

Abstract

Multiple arteriovenous malformations (AVMs) are uncommon, accounting for only 0.3-3.2% of all AVM cases. These AVMs are often found in syndromic pediatrics of HHT and WMS. Consideration of the patient's condition, the angioarchitecture of each AVM, and the hemodynamic connection of AVMs is crucial in determining the optimal therapeutic approach. However, the optimal therapeutic decision-making for these complex vascular lesions can be challenging due to the scarcity of their reports and their long-term follow-up. In this report, we present the case of a young man who presented with a headache, and DSA shows three left parietal AVMs, each with a separate nidus, feeder artery, and draining vein.

摘要

多发性动静脉畸形(AVM)并不常见,仅占所有AVM病例的0.3%-3.2%。这些AVM常见于遗传性出血性毛细血管扩张症(HHT)和Wyburn-Mason综合征(WMS)的综合征性儿科患者中。考虑患者的病情、每个AVM的血管构筑以及AVM之间的血流动力学联系对于确定最佳治疗方法至关重要。然而,由于关于这些复杂血管病变的报告稀缺且缺乏长期随访,因此针对它们的最佳治疗决策可能具有挑战性。在本报告中,我们介绍了一名出现头痛的年轻男性病例,数字减影血管造影(DSA)显示左侧顶叶有三个AVM,每个都有独立的病灶、供血动脉和引流静脉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd81/11695499/eb0fd2431667/jcen-2024-e2024-05-002f1.jpg

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