Japanese Journal of Vascular Surgery
Online ISSN : 1881-767X
Print ISSN : 0918-6778
Case Reports
A Case of Bilateral Axillary Artery Aneurysms Caused by Fibromuscular Dysplasia
Takaaki Saito Kazunori InuzukaMasaki SanoNaoki UnnoNaoto YamamotoHiroya Takeuchi
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JOURNAL OPEN ACCESS

2018 Volume 27 Issue 3 Pages 209-212

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Abstract

Axillary artery aneurysm is rare. Although there were some reports that this disease was caused by repeated trauma and iatrogenic factor, thoracic outlet syndrome and systemic disease like Marfan syndrome, the cause by fibromuscular dysplasia (FMD) is extremely rare. A 68-year-old woman had complaint of a fever and she was diagnosed as bilateral axillary artery aneurysms by contrast-enhanced computed tomography in another hospital, she was referred to our hospital. On general anesthesia and supine position, we achieved replacement of both aneurysms with 8 mm externally supported knitted Dacron grafts (Gelsoft ERS) using the subclavian approach. Histopathological examination revealed the aneurysm wall had neither arteriosclerosis nor arteritis. The elastic fibers of intima were thickened (intimal fibroplasia), those of media were irregular and sparse (medial fibromuscular dysplasia), adventitia was normal, these findings corresponded to FMD. At first year after operation, there is no recurrence of aneurysms, grafts are patency.

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この記事はクリエイティブ・コモンズ [表示 - 非営利 - 継承 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-sa/4.0/deed.ja
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