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作为白塞病的一种结局或作为一种不同疾病实体的休斯-斯托文综合征。

Hughes-Stovin Syndrome as an Outcome of Behçet Disease or as a Different Entity.

作者信息

Demirkan Serkan, Gültekin Yıldırım

机构信息

Department of Dermatology and Venerology, Kirikkale University Faculty of Medicine.

Department of Cardiovascular Surgery, Kirikkale University Faculty of Medicine.

出版信息

Korean J Thorac Cardiovasc Surg. 2018 Feb;51(1):64-68. doi: 10.5090/kjtcs.2018.51.1.64. Epub 2018 Feb 5.

Abstract

Hughes-Stovin syndrome is a rare disorder of unknown etiology. Although the association between multiple pulmonary artery aneurysms and venous thrombosis of the lower limbs was reported by Beattie and Hall in 1911, it was not until 1962 that the eponym "Hughes-Stovin syndrome" was formally introduced in the medical literature. We describe 2 patients with Hughes-Stovin syndrome who presented with pulmonary artery aneurysm, thrombophlebitis, hemoptysis, and oral ulcers, review the manifestations of the disease, and compare its similarities with and differences from Behçet disease.

摘要

休斯-斯托文综合征是一种病因不明的罕见疾病。尽管1911年贝蒂和霍尔报告了多发性肺动脉瘤与下肢静脉血栓形成之间的关联,但直到1962年,“休斯-斯托文综合征”这一名称才正式出现在医学文献中。我们描述了2例患有休斯-斯托文综合征的患者,他们表现为肺动脉瘤、血栓性静脉炎、咯血和口腔溃疡,回顾了该疾病的临床表现,并比较了其与白塞病的异同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/211f/5796621/1f285e99ef66/kjtcv-51-064f1.jpg

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