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:: Volume 8, Issue 4 (7-2017) ::
Caspian J Intern Med 2017, 8(4): 332-334 Back to browse issues page
Hughes-Stovin syndrome revealing the presence of Behçet’s Disease
Melek Kechida *, Sondes Yaacoubi , Ahmed Zrig , Walid Jomaa , Rim Klii , Sonia Hammami , Ines Khochtali
MD Department of Internal Medicine and Endocrinology, Fattouma Bourguiba Hospital, University of Monastir, Tunisia , kechida_mel_lek@hotmail.com
Abstract:   (563 Views)
Background: Hughes-Stovin Syndrome (HSS) is a rare clinical disorder characterized by deep venous thrombosis and multiple pulmonary and/or bronchial aneurysms. Aneurysms in systemic circulation can also be seen.
Case presentation: We report the first case of HSS with aortic aneurysm in a 55-year-old man who initially presented with deep venous thrombosis. The diagnosis of HSS revealing Behçet’s disease was made given the history of recurrent oral and genital ulcers. Treatment consisted of 3 daily pulses of methylprednisolone (1g) followed by oral prednisone (1mg/kg daily) and 6 monthly pulses of cyclophosphamide. Oral anticoagulation treatment was  held  3 months and then was stopped with good outcome.
Conclusion: Systemic aneurysms in Hughes Stovin is a worth knowing complication which may reveal Behçet’s disease.

Keywords: Behçet syndrome, Hughes-Stovin syndrome, Aortic aneurysm
Full-Text [PDF 209 kb]   (119 Downloads)    
Type of Study: case report | Subject: Internal
Received: 2016/09/22 | Accepted: 2017/04/29 | Published: 2017/09/19
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DOI: 10.22088/cjim.8.4.332


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Kechida M, Yaacoubi S, Zrig A, Jomaa W, Klii R, Hammami S et al . Hughes-Stovin syndrome revealing the presence of Behçet’s Disease . Caspian J Intern Med. 2017; 8 (4) :332-334
URL: http://caspjim.com/article-1-871-en.html
Volume 8, Issue 4 (7-2017) Back to browse issues page
Caspian Journal of Internal Medicine
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