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Spontaneous Rupture of Multiple Occipital Artery Aneurysms in a Patient With Neurofibromatosis Type 1

机译:患有神经纤维瘤病患者的多发性动脉动脉瘤的自发破裂1

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摘要

Neurofibromatosis type 1 (NF-1) is an autosomal dominant genetic disorder, mainly characterized by skin and peripheral nervous system abnormalities. Uncommonly, NF-1 may be associated with peripheral or supra-aortic trunks artery aneurysms. We report a case of symptomatic multiple occipital artery aneurysms detected in a 53-year-old woman affected by sporadic NF-1. An endovascular approach was performed to exclude aneurysms and to stop laterocervical spontaneous hematoma.
机译:神经纤维瘤病1(NF-1)是一种常染色体显性遗传症,主要是皮肤和周围神经系统异常的特征。 罕见地,NF-1可以与外周或超主动脉裤动脉瘤相关联。 我们在受零星NF-1影响的53岁女性中举报了对症状多发性动脉动脉瘤的病例。 进行血管内方法以排除动脉瘤并止止伴咽性自发性血肿。

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