1型神经纤维瘤病所致颈外动脉瘤及瘘口破裂的成功治疗:附2例报告

IF 0.3 Q4 OTORHINOLARYNGOLOGY
Ryutaro Onaga, Toru Sasaki, Tomohiko Yamauchi, K. Namba, A. Higaki, A. Gomi, H. Nishino
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引用次数: 0

摘要

摘要1型神经纤维瘤病是一种遗传性疾病。血管畸形是轻微的并发症,但破裂是致命的。我们报告了两例颅外颈动脉破裂血管畸形,在成功治疗后存活下来。病例1是一名35岁的男性,由于咽部肿块导致气道阻塞。肿块被诊断为右颈内动脉瘤破裂。对颞浅动脉-大脑中动脉(STA-MCA)搭桥术后右颈内动脉血管内闭塞进行了紧急治疗。病例2是一名55岁的男性,他表现出与右侧颈部肿胀相关的呼吸困难。血管造影显示两个主要的高流量动静脉瘘,主要来自ICA和上颌动脉。患者还接受了栓塞治疗。对这些罕见病例的早期诊断和适当的治疗可以挽救严重病情后的生命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful treatment of ruptured extracranial carotid artery aneurysm and fistula associated with neurofibromatosis type1: Report of two cases
Abstract Neurofibromatosis type 1 is an inherited disease. Vascular malformation represents minor complication but the rupture is fatal. We report two cases of ruptured vascular malformation in extracranial carotid artery who survived after successful treatment. Case 1 was a 35-year-old man who presented with airway obstruction due to a mass in the pharynx. The mass was diagnosed as ruptured aneurysm of the right internal carotid artery (ICA). An emergent treatment of superficial temporal artery to middle cerebral artery (STA–MCA) bypass surgery followed by endovascular occlusion of the right ICA was conducted. Case 2 was a 55-year-old man who presented with dyspnea associated with right-side neck swelling. Angiography showed two major high-flow arteriovenous fistulas, mainly fed from the ICA and maxillary artery. The patient also underwent embolization. Early diagnoses and appropriate managements of these rare cases could save lives after the serious condition.
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