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Thrombosis in Beh?et's disease: a Beh?et's disease patient with complete thrombotic obstruction of IVC and both iliac veins and decreased protein S activity

Authors
LEE YOUNG HOJi Jong DaeGwan Gyu SongChung Hwan Hoonsungjae Choi
Issue Date
12월-2011
Publisher
Springer Verlag
Citation
RHEUMATOLOGY INTERNATIONAL, v.0, no.0, pp.0 - 0
Indexed
SCIE
SCOPUS
Journal Title
RHEUMATOLOGY INTERNATIONAL
Volume
0
Number
0
Start Page
0
End Page
0
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/84569
ISSN
0172-8172
Abstract
Beh?et`s disease represents a multisystemic inflammatory disease characterized by recurrent oral ulcers, genital ulcers, and uveitis. Although vascular attack and thrombosis are not major complications in Beh?et`s disease, they can still pose risks that must not be overlooked. In this paper, we reported that a 25-year-old female Beh?et`s disease patient with complete thrombotic obstruction of the inferior vena cava that was successfully treated by aspiration thrombectomy and balloon angioplasty. The procedure produced marked symptomatic improvement. Currently, data about the treatment and the prophylaxis of thrombotic events in Beh?et`s disease are lacking. In this case report, we hope to discuss the future direction of such studies, how we understand the mechanism of Beh?et`s disease hypercoagulability, and which treatments can improve thrombotic tendencies in Beh?et`s disease. ? 2011 Springer-Verlag.
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