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1 型神经纤维瘤病并发有潜在生命威胁性血栓形成的罕见颈内静脉动脉瘤样变性。

A rare case of internal jugular vein aneurysmal degeneration in a type 1 neurofibromatosis complicated by potentially life-threatening thrombosis.

机构信息

Vascular Surgery Unit, Misericordia Hospital, Grosseto, Italy.

出版信息

J Vasc Surg. 2011 Oct;54(4):1170-3. doi: 10.1016/j.jvs.2011.03.273.

Abstract

Type 1 neurofibromatosis (NF1) is an autosomal dominant disorder characterized by multiple forms of neural crest cell proliferation. Associated venous malformations are extremely rare. We present a case of a giant thrombosed internal jugular aneurysm with brachiocephalic vein thrombosis in an NF1 patient. Surgical correction required prophylactic left brachiocephalic vein ligation, aneurysm evacuation, and proximal jugular vein ligation. Extreme vein friability caused severe intraoperative bleeding. Vein wall histology confirmed neurofibromatosis infiltration. Jugular vein aneurysm and infiltration in NF1, although exceedingly rare, can pose a serious threat to the patient during surgical correction, with major vessel thrombosis enhancing morbidity and mortality.

摘要

1 型神经纤维瘤病(NF1)是一种常染色体显性遗传病,其特征是多种神经嵴细胞增殖。相关的静脉畸形极为罕见。我们报告一例 NF1 患者发生巨大血栓形成的颈内静脉动脉瘤合并头臂静脉血栓形成。手术矫正需要预防性结扎左侧头臂静脉、动脉瘤排空和颈内静脉近端结扎。静脉壁极度脆弱导致术中严重出血。静脉壁组织学证实为神经纤维瘤病浸润。尽管颈内静脉动脉瘤和 NF1 浸润极为罕见,但在手术矫正过程中会对患者造成严重威胁,主要血管血栓形成会增加发病率和死亡率。

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