Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis -- case report.

Abstract:

:Behçet's disease is a chronic inflammatory disease of unknown aetiology, characterized by recurrent oral and genital aphthous ulcerations, uveitis, skin lesions and other multisystem affections associated with vasculitis. Different types of vessels, predominantly veins, can be affected in Behçet's disease. The frequency of vascular lesions in Behçet's disease, such as superficial and deep venous thromboses, arterial aneurysms and occlusions, ranges between 7-29%. Budd-Chiari syndrome is a rare and serious complication of Behçet's disease and implies thrombosis of the hepatic veins and/or the intrahepatic or suprahepatic inferior vena cava. We report a case of a 25-year-old man with Behçet's disease that developed Budd-Chiari syndrome. The correlation of dermatological, pathological and imaging studies confirmed the diagnosis.

journal_name

An Bras Dermatol

authors

Bittencourt Mde J,Dias CM,Lage TL,Barros RS,Paz OA,Vieira Wde B

doi

10.1590/abd1806-4841.20131930

subject

Has Abstract

pub_date

2013-05-01 00:00:00

pages

448-51

issue

3

eissn

0365-0596

issn

1806-4841

pii

S0365-05962013000300448

journal_volume

88

pub_type

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