Literature DB >> 15071462

Rupture of the abdominal aorta in a 13-year-old girl secondary to Behçet disease: a case report.

Veysel Kutay1, Cevat Yakut, Hasan Ekim.   

Abstract

Behçet 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-Behçet disease with a ruptured abdominal aortic aneurysm without a formerly known history of Behçet disease. Urgent aortoiliac bypass with a polytetrafluoroethylene graft was performed with success, and the patient has also received corticosteroid and immunosuppressive drug therapy.

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Year:  2004        PMID: 15071462     DOI: 10.1016/j.jvs.2003.12.020

Source DB:  PubMed          Journal:  J Vasc Surg        ISSN: 0741-5214            Impact factor:   4.268


  2 in total

1.  Emergent stent-graft repair of a massive aortic pseudoaneurysm secondary to Behçet's disease in a child.

Authors:  Allison Dawson; Giri M Shivaram; Sarah K Baxter; Eric J Monroe; Kevin S H Koo
Journal:  Diagn Interv Radiol       Date:  2018-09       Impact factor: 2.630

2.  Endovascular treatment of aortic saccular aneurysms associated with Adamantiades-Behçet disease.

Authors:  Patrick Bastos Metzger; Kamilla Rosales Costa; Simone Lessa Metzger; Leonardo Cortizo de Almeida
Journal:  J Vasc Bras       Date:  2021-06-25
  2 in total

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