| Literature DB >> 32010896 |
Nükhet Aladağ Çiftdemir1, Selman Gökalp2, Tuba Eren1.
Abstract
Behçet's disease (BD) is a rare, multisystemic, chronic vasculitic disorder with unknown etiology. Intracardiac thrombus formation and pulmonary artery aneurysm in BD are very rare. The treatment protocol in patients with vascular involvement, particularly those with pulmonary artery aneurysm accompanied by thrombosis, have not been clearly defined. In this article, we report an exceptional case, who had been treated unsuccessfully with a combination of anti-inflammatory/immunosuppressive therapy and thrombolytic agents, to discuss the poor prognosis of pulmonary artery aneurysm accompanying intracardiac thrombosis in juvenile BD.Entities:
Keywords: Behçet’s disease; intracardiac thrombosis; pulmonary artery aneurysm
Year: 2019 PMID: 32010896 PMCID: PMC6974390 DOI: 10.5606/ArchRheumatol.2019.7169
Source DB: PubMed Journal: Arch Rheumatol ISSN: 2148-5046 Impact factor: 1.472