A Rare Case of Hughes-Stovin Syndrome Presenting with Ischemic Colitis Caused by an Arteriovenous Malformation.

IF 1.1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Internal Medicine Pub Date : 2025-10-15 Epub Date: 2025-04-12 DOI:10.2169/internalmedicine.5185-24
Kazuya Maruo, Makoto Tanaka, Yutaka Inada, Akifumi Fukui, Naoya Tomatsuri, Hideki Sato, Osamu Inamori, Masanori Yamashita, Katsuhiko Oka, Yusuke Okuyama
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引用次数: 0

Abstract

Hughes-Stovin syndrome (HSS) is an exceedingly rare disease characterized by thrombotic phlebitis and pulmonary or bronchial artery aneurysms. A 68-year-old man presented with ischemic colitis, and angiography revealed occlusion of the inferior mesenteric vein and arteriovenous malformation in the inferior mesenteric artery region. Medical treatment was unsuccessful, and a left hemicolectomy was therefore performed following coil embolization. Subsequently, a pulmonary artery aneurysm was incidentally detected, and coil embolization was performed. However, the patient developed deep vein thrombosis and a pulmonary embolism, which led to a diagnosis of HSS. To our knowledge, this is the first report of ischemic colitis as a presenting feature of HSS.

一例罕见的休斯-斯托文综合征,表现为由动静脉畸形引起的缺血性结肠炎。
休斯-斯托文综合征(HSS)是一种极其罕见的疾病,其特征是血栓性静脉炎和肺或支气管动脉动脉瘤。一名68岁男性患者因缺血性结肠炎就诊,血管造影显示肠系膜下静脉闭塞,肠系膜下动脉区动静脉畸形。药物治疗不成功,因此在线圈栓塞后进行左结肠切除术。随后,偶然发现肺动脉动脉瘤,并进行了线圈栓塞术。然而,患者出现了深静脉血栓和肺栓塞,这导致了HSS的诊断。据我们所知,这是首次报道缺血性结肠炎作为HSS的表现特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Internal Medicine
Internal Medicine 医学-医学:内科
CiteScore
1.90
自引率
8.30%
发文量
0
审稿时长
2.2 months
期刊介绍: Internal Medicine is an open-access online only journal published monthly by the Japanese Society of Internal Medicine. Articles must be prepared in accordance with "The Uniform Requirements for Manuscripts Submitted to Biomedical Journals (see Annals of Internal Medicine 108: 258-265, 1988), must be contributed solely to the Internal Medicine, and become the property of the Japanese Society of Internal Medicine. Statements contained therein are the responsibility of the author(s). The Society reserves copyright and renewal on all published material and such material may not be reproduced in any form without the written permission of the Society.
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