Kutay, VYakut, CEkim, H2025-05-102025-05-1020040741-521410.1016/j.jvs.2003.12.0202-s2.0-1642464758https://doi.org/10.1016/j.jvs.2003.12.020https://hdl.handle.net/20.500.14720/14816Kutay, Veysel/0000-0002-5822-5259Behcet 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.eninfo:eu-repo/semantics/openAccessArticle394Q1Q190190215071462WOS:000227387300039