New Search

Export article

Double aortic dissection in a patient with Marfan disease. A case report

Christian Millogo Georges Rosa, Koudougou Kologo Jonas, Arthur Seghda Taryètba André, Théodore Boro, Laurence Benon, K Samadoulougou André, Patrice Zabsonré

Abstract: Marfan syndrome is a dominant autosomal genetic disease of the connective tissue, leading to various complications. Cardiovascular complications are the main ones, with dilation of the aorta and aortic dissection which is the main cause of death. Double dissection with different sites of departure is scarcely reported by the literature. We reported the case of a 22-year’s-old young patient admitted for acute chest and abdominal pains, and cardiogenic shock. Investigations reported a double dissection of the aorta with a recent one of type A and an old one of type B. Ghent diagnostic criteria were used to allow the diagnosis of Marfan disease. Surgical management corrected successfully the type A dissection. Early diagnostic and adequate management of aortic complications can reduce the high mortality rate of patients with Marfan syndrome.
Keywords: Marfan disease / old / aorta / complications / aortic dissection / double dissection

Scifeed alert for new publications

Never miss any articles matching your research from any publisher
  • Get alerts for new papers matching your research
  • Find out the new papers from selected authors
  • Updated daily for 49'000+ journals and 6000+ publishers
  • Define your Scifeed now

Share this article

Click here to see the statistics on "Journal of Cardiology and Cardiovascular Medicine" .
References (17)
    Back to Top Top