دوره 8، شماره 4 - ( 4-1396 )                   جلد 8 شماره 4 صفحات 334-332 | برگشت به فهرست نسخه ها


XML English Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

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-fa.html
Hughes-Stovin syndrome revealing the presence of Behçet’s Disease . . 1396; 8 (4) :332-334

URL: http://caspjim.com/article-1-871-fa.html


چکیده:   (7202 مشاهده)
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.

متن کامل [PDF 209 kb]   (1105 دریافت)    
نوع مطالعه: case report | موضوع مقاله: Internal
دریافت: 1395/7/1 | پذیرش: 1396/2/9 | انتشار: 1396/6/28

ارسال نظر درباره این مقاله : نام کاربری یا پست الکترونیک شما:
CAPTCHA

بازنشر اطلاعات
Creative Commons License این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است.

کلیه حقوق این وب سایت متعلق به می باشد.

طراحی و برنامه نویسی : یکتاوب افزار شرق

© 2025 CC BY-NC 4.0 | Caspian Journal of Internal Medicine

Designed & Developed by : Yektaweb