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Rupture of the Abdominal Aorta in a 13-Year Girl Secondary To Behcet Disease: a Case Report

dc.authorid Kutay, Veysel/0000-0002-5822-5259
dc.authorscopusid 6602259733
dc.authorscopusid 7005925621
dc.authorscopusid 55931157400
dc.contributor.author Kutay, V
dc.contributor.author Yakut, C
dc.contributor.author Ekim, H
dc.date.accessioned 2025-05-10T17:39:16Z
dc.date.available 2025-05-10T17:39:16Z
dc.date.issued 2004
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Yuzuncu Yil Univ, Fac Med, Cardiovasc Surg Clin, Van, Turkey en_US
dc.description Kutay, Veysel/0000-0002-5822-5259 en_US
dc.description.abstract Behcet disease is a multisystemic vasculitis of unknown origin. The vascular complications as a result of the disease are rare in the pediatric age group. We report a 13-year-old patient with vasculo-Behcet disease with a ruptured abdominal aortic aneurysm without a formerly known history of Beh et disease. Urgent aortoiliac bypass with a polytetrafluoroethylene graft was performed with success, and the patient has also received corticosteroid and immunosuppressive drug therapy. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1016/j.jvs.2003.12.020
dc.identifier.endpage 902 en_US
dc.identifier.issn 0741-5214
dc.identifier.issue 4 en_US
dc.identifier.pmid 15071462
dc.identifier.scopus 2-s2.0-1642464758
dc.identifier.scopusquality Q1
dc.identifier.startpage 901 en_US
dc.identifier.uri https://doi.org/10.1016/j.jvs.2003.12.020
dc.identifier.uri https://hdl.handle.net/20.500.14720/14816
dc.identifier.volume 39 en_US
dc.identifier.wos WOS:000227387300039
dc.identifier.wosquality Q1
dc.language.iso en en_US
dc.publisher Mosby, inc en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Rupture of the Abdominal Aorta in a 13-Year Girl Secondary To Behcet Disease: a Case Report en_US
dc.type Article en_US

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