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Superior vena cava syndrome revealing a Behçet’s disease

2015; BioMed Central; Volume: 13; Issue: 1 Linguagem: Inglês

10.1186/s12959-015-0039-z

1477-9560

Simon Antoine Sarr, Pape Diadié Fall, Mouhamadou Chérif Mboup, Khadidiatou Dia, Malick Bodian, Modou Jobe,

Retinal and Optic Conditions

Behçet's disease (BD) is a rare vasculitis in sub-Saharan Africa. Vascular thrombosis, especially venous, is common in this condition and also constitutes a basic diagnostic criterion. Its affection of the superior vena cava is rather rare with only a few cases described in the literature.A 42-year-old male patient was seen at consultation presenting with a pulsatile, warm and slightly painful right latero-cervical swelling extending to the supraclavicular fossa with the presence of collateral venous circulation for three weeks prior to presentation associated with a mild headache. There were oral and genital ulcerations and erythematous skin lesions associated with a history of inflammatory recurrent arthralgia. Chest computed tomo-angiography showed cruoric internal jugular vein thrombosis extending to the superior vena cava with significant venous collateral circulation. The patient was treated with prednisolone (1 mg/kg/day) and colchicine (2 mg/day), as well as anticoagulation with heparin and vitamin K antagonist (Acenocoumarol) with regular INR monitoring. Clinical evolution was favorable during hospitalization, with residual discrete right supraclavicular swelling. There was no bleeding associated with anticoagulants use.The case stresses the importance of maintaining a high degree of suspicion for Behçet's disease in all cases of venous thrombosis.