首页> 外文期刊>Neurologia medico-chirurgica. >Ruptured large basilar artery aneurysm associated with an arteriovenous malformation in hereditary hemorrhagic telangiectasia
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Ruptured large basilar artery aneurysm associated with an arteriovenous malformation in hereditary hemorrhagic telangiectasia

机译:与遗传性出血性毛细血管扩张相关的动静脉畸形伴有破裂的基底大动脉瘤破裂

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摘要

A 53-year-old woman presented with intracranial hemorrhage caused by a ruptured cerebral aneurysm. Digital subtraction angiography revealed a large aneurysm arising from the top of the basilar artery and a Spetzler-Martin grade 3 arteriovenous malformation. Endovascular embolization of the aneurysm was completed with a slight neck remnant. Medical examination confirmed that she suffered from hereditary hemorrhagic telangiectasia (HHT). HHT is a rare autosomal dominant disorder characterized by multiple mucocutaneous telangiectasia and associated vascular malformations. This case suggests that the prognosis for HHT patients with treatable aneurysms should be as good as that of healthy individuals. Consequently, neurosurgeons should suspect underlying HHT in all patients with cerebral vascular malformations.
机译:一名53岁的妇女因脑动脉瘤破裂而出现颅内出血。数字减影血管造影显示基底动脉顶部出现大动脉瘤和Spetzler-Martin 3级动静脉畸形。动脉瘤的血管内栓塞已完成,颈部轻微残留。体格检查证实她患有遗传性出血性毛细血管扩张症(HHT)。 HHT是一种罕见的常染色体显性遗传疾病,其特征是多发性皮肤粘膜毛细血管扩张和相关的血管畸形。该病例表明,患有可治疗的动脉瘤的HHT患者的预后应与健康个体的预后相同。因此,神经外科医师应怀疑所有脑血管畸形患者的潜在HHT。

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