Literature DB >> 9112886

Superior vena cava syndrome as a primary manifestation of Behçet's disease. A case report.

A Roguin1, S Edelstein, Y Edoute.   

Abstract

Superficial thrombophlebitis is a common finding in Behçet's disease. However, the potential life-threatening complication of superior vena cava (SVC) syndrome due to thrombotic occlusion is a rare manifestation and usually occurs several years after the onset of the diagnosis. The authors describe a twenty-nine-year-old Arab man who had an acute thrombosis of the SVC as the presenting manifestation of his Behçet's disease. The patient was successfully treated with thrombolytic and anticoagulant therapy, and during follow-up no relapse was observed. Behçet's disease should be suspected in young patients presenting with thrombosis of the SVC and without evidence of a hypercoagulable state.

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Year:  1997        PMID: 9112886     DOI: 10.1177/000331979704800411

Source DB:  PubMed          Journal:  Angiology        ISSN: 0003-3197            Impact factor:   3.619


  2 in total

1.  Superior vena cava syndrome: a rare clinical manifestation of Behcet's disease.

Authors:  Ismail Hanta; Gamze Ucar; Sedat Kuleci; Süleyman Ozbek; Ali Kocabas
Journal:  Clin Rheumatol       Date:  2004-09-02       Impact factor: 2.980

2.  Behçet's disease associated with superior vena cava syndrome without thrombosis.

Authors:  Tadeu Ferreira de Paiva; Henrique Barbosa Ribeiro; Cristiano Barbosa Campanholo; Célio Roberto Gonçalves; Dawton Y Terigoe; Branca Dias Batista de Souza
Journal:  Clin Rheumatol       Date:  2006-03-15       Impact factor: 2.980

  2 in total

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