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以广泛胸腹主动脉瘤为首发表现的大动脉炎:病例系列及文献综述

Extensive thoracoabdominal aortic aneurysm as initial presentation in Takayasu arteritis: case series and literature review.

作者信息

Jena Anupam, Mishra Subasis, Padhee Binayananda, Jena Surya Kant, Ghosh Nelson, Padhan Prasanta, Rout Nikunja Kishore, Sahoo Panchanan

机构信息

Department of Cardiology, Kalinga Institute of Medical Sciences, Campus 5, KIIT University, Patia, Bhubaneswar, India.

Department of Immunology, Kalinga Institute of Medical Sciences, KIIT University, Patia, Bhubaneswar, India.

出版信息

Eur Heart J Case Rep. 2023 Dec 18;8(1):ytad627. doi: 10.1093/ehjcr/ytad627. eCollection 2024 Jan.

Abstract

BACKGROUND

Aortic aneurysm as a presenting feature in Takayasu's arteritis is very rare. Here, we report three cases of extensive thoracoabdominal aortic aneurysm in Takayasu's arteritis as initial presentation.

CASE SUMMARY

All three cases were males and presented with complaints of abdominal pain and refractory hypertension. The diagnosis was made from the finding of thickened and calcified aortic wall, stenosis of visceral arteries, and age < 40 years at diagnosis. Case 1 was a 34 years male with aortic aneurysm extending from left subclavian artery to infrarenal aorta. He underwent endovascular repair of aneurysm by sandwich chimney technique in view of impending aneurysm rupture. Case 2, a 37 years male had aortic aneurysm from descending thoracic aorta (D4 vertebral body) to infrarenal aorta (L4 level). While being evaluated for repair, he had sudden death probably due to ruptured aneurysm. Case three, a 40 years male had aortic aneurysm extending from left subclavian artery to aortic bifurcation and stenosis of visceral arteries. He did not consent for repair and died one year later due to chronic kidney disease and related complications.

DISCUSSION

Thoracoabdominal aortic aneurysm is a very rare manifestation in Takayasu's arteritis; more common in males. Endovascular repair is challenging but feasible. Long-term monitoring and repeat intervention may be needed due to young age of patients and disease progression.

摘要

背景

主动脉瘤作为大动脉炎的首发表现非常罕见。在此,我们报告3例大动脉炎患者以广泛胸腹主动脉瘤为初始表现的病例。

病例摘要

所有3例均为男性,均以腹痛和顽固性高血压为主要症状。根据主动脉壁增厚钙化、内脏动脉狭窄以及诊断时年龄<40岁的表现做出诊断。病例1为一名34岁男性,主动脉瘤从左锁骨下动脉延伸至肾下主动脉。鉴于动脉瘤即将破裂,他接受了三明治烟囱技术的动脉瘤腔内修复术。病例2为一名37岁男性,主动脉瘤从胸降主动脉(第4椎体)延伸至肾下主动脉(第4腰椎水平)。在评估修复时,他突然死亡,可能是由于动脉瘤破裂。病例3为一名40岁男性,主动脉瘤从左锁骨下动脉延伸至主动脉分叉,伴有内脏动脉狭窄。他不同意修复,一年后因慢性肾病及相关并发症死亡。

讨论

胸腹主动脉瘤在大动脉炎中是一种非常罕见的表现;在男性中更为常见。腔内修复具有挑战性,但可行。由于患者年龄较轻且疾病进展,可能需要长期监测和重复干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c658/10766067/f7207f283fb1/ytad627f9.jpg

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