手术修复巨大下腔静脉动脉瘤合并先天性血管异常1例报告。

IF 0.8 Q4 PERIPHERAL VASCULAR DISEASE
Konstantinos Dimitriadis, Nikolaos Papatheodorou, Nikolaos Triantafyllou, Stavros Parisidis, Christos Argyriou, George S Georgiadis
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引用次数: 0

摘要

下腔静脉动脉瘤(IVCAs)是罕见但潜在致命的,特别是如果他们有症状或并发症。在文献报道的ivca中,只有少数与先天性血管异常有关,包括先天性IVC梗阻、法洛四联症、左侧IVC、重复IVC、ehers - danlos综合征、蓝橡胶泡痣综合征和Klipper-Trenaunay综合征。我们提出的病例8厘米症状性囊性IVCA患者法洛四联症,治疗成功的手术修复。虽然罕见的静脉病变有时可以通过血管内治疗来治疗,但开放手术重建仍然是持久和最终修复的主要方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgical Repair of a Giant Inferior Vena Cava Aneurysm Associated with a Congenital Vascular Anomaly: A Case Report.

Inferior vena cava aneurysms (IVCAs) are rare yet potentially lethal, especially if they are symptomatic or complicated. Among the IVCAs reported in the literature, only a few are associated with congenital vascular anomalies, including congenital IVC obstruction, tetralogy of Fallot, left-sided IVC, duplicated IVC, Ehlers-Danlos syndrome, blue rubber bleb nevus syndrome, and Klipper-Trenaunay syndrome. We present the case of an 8-cm symptomatic saccular IVCA in a patient with tetralogy of Fallot, treated successfully with surgical repair. Although rare venous pathologies can sometimes be managed with endovascular treatment, open surgical reconstruction remains the mainstay of durable and definitive repair.

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来源期刊
CiteScore
1.10
自引率
11.10%
发文量
29
审稿时长
17 weeks
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