多发性动静脉畸形伴单独的尼迪,病例报告和文献综述。

Morteza Taheri, Aryoobarzan Rahmatian, Parisa Javadnia
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引用次数: 0

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%。这些动静脉畸形通常出现在 HHT 和 WMS 的综合征儿科病例中。考虑患者的病情、每种 AVM 的血管结构以及 AVM 的血液动力学联系对于确定最佳治疗方法至关重要。然而,由于相关报告和长期随访的稀缺性,针对这些复杂血管病变的最佳治疗决策可能具有挑战性。在本报告中,我们介绍了一名年轻男子的病例,他因头痛而就诊,DSA 显示其左顶叶有三个 AVM,每个都有独立的巢穴、馈动脉和引流静脉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple AVM with separate nidi, a case report and review the literatures.

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.

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