| Literature DB >> 20868576 |
Gerard Espinosa1, Isabel Blanco, Juan Miguel Antón, Marcelo Sánchez, Paolo Macchiarini, Joan Albert Barberà.
Abstract
Behçet's disease is a systemic vasculitis characterised by recurrent mouth and genital ulcers and uveitis. About 25% of patients suffer from vascular involvement. We describe a patient with Behçet's disease who suffered recurrent pulmonary embolism and developed severe chronic thromboembolic pulmonary hypertension. The patient was successfully treated with pulmonary endarterectomy that normalised pulmonary haemodynamics. Chronic thromboembolic pulmonary hypertension is a potential complication of Behçet's disease that may be amenable to pulmonary endarterectomy.Entities:
Mesh:
Year: 2010 PMID: 20868576
Source DB: PubMed Journal: Clin Exp Rheumatol ISSN: 0392-856X Impact factor: 4.473