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 |