{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,4,27]],"date-time":"2025-04-27T14:10:09Z","timestamp":1745763009541,"version":"3.40.4"},"reference-count":15,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2015,7,12]]},"abstract":"<jats:p>Beh\u00e7et's disease is an autoimmune mediated multisystem vasculitis. It is most prevalent in Middle Eastern and Mediterranean patients and considered rare in Afro-Caribbean populations. The disease phenotype in Afro-Caribbean patients is more severe with systemic involvement, in particular lesions affecting the vascular system known as angio-Beh\u00e7et's. The archetypal triad of disease in Beh\u00e7et's includes oral stomatitis, genital ulceration and ocular lesions, however, the variety of symptoms patients experience is recognised by the revised International Criteria for Beh\u00e7et's disease and is reflected in the clinical scoring criteria. The authors report an unusual case of Beh\u00e7et's disease in a young Afro-Caribbean patient presenting with spontaneous bilateral renal, cerebral and pulmonary venous thrombosis as first presentation. Physicians should be aware of the aggressive and atypical manner in which Beh\u00e7et's can present in Afro-Caribbean patients in order to avoid diagnostic delay and remain vigilant for thromboembolic lesions in this population.<\/jats:p>","DOI":"10.1136\/bcr-2015-211195","type":"journal-article","created":{"date-parts":[[2015,7,23]],"date-time":"2015-07-23T15:13:44Z","timestamp":1437664424000},"page":"bcr2015211195","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":0,"title":["Spontaneous multisystem deep venous thrombosis as an unusual presentation of Beh\u00e7et's disease in a young Afro-Caribbean patient"],"prefix":"10.1136","volume":"2015","author":[{"given":"Anuja","family":"Mitra","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2015,7,23]]},"reference":[{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.1","doi-asserted-by":"publisher","DOI":"10.1111\/jdv.12107"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.2","first-page":"1033","article-title":"Behcet's disease in Israel: the influence of ethnic origin on disease expression and severity","volume":"28","author":"Krause","year":"2001","journal-title":"J Rheumatol"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.3","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajem.2013.07.037"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.4","doi-asserted-by":"publisher","DOI":"10.1007\/s10067-010-1430-6"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.5","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199910213411707"},{"issue":"(Suppl 2)","key":"2025042706510644000_2015.jul23_1.bcr2015211195.6","first-page":"1086","article-title":"A case of extensive recalcitrant IVC thrombosis in a teenager with Behcet disease","volume":"11","author":"Nakar","year":"2013","journal-title":"J Thromb Haemost"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.7","doi-asserted-by":"publisher","DOI":"10.1177\/0003319707303891"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.8","first-page":"858","article-title":"Budd-Chiari syndrome: a common complication of Behcet's disease","volume":"92","author":"Bayraktar","year":"1997","journal-title":"Am J Gastroenterol"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.9","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-009-0145-6"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.10","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/122.11.2171"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.11","doi-asserted-by":"publisher","DOI":"10.1097\/00005382-199422000-00012"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.12","doi-asserted-by":"publisher","DOI":"10.3109\/14397595.2013.843751"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.13","doi-asserted-by":"publisher","DOI":"10.1136\/bjo.87.7.876"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.14","doi-asserted-by":"publisher","DOI":"10.1007\/s004150200031"},{"key":"2025042706510644000_2015.jul23_1.bcr2015211195.15","doi-asserted-by":"publisher","DOI":"10.1093\/rheumatology\/36.4.498"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2015-211195","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,27]],"date-time":"2025-04-27T13:51:12Z","timestamp":1745761872000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2015-211195"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,7,23]]},"references-count":15,"alternative-id":["10.1136\/bcr-2015-211195"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2015-211195","relation":{},"ISSN":["1757-790X"],"issn-type":[{"type":"electronic","value":"1757-790X"}],"subject":[],"published":{"date-parts":[[2015,7,23]]}}}