Surgical treatment of siblings with Marfan syndrome
Asian Cardiovascular and Thoracic Annals, cilt.7, sa.2, ss.138-141, 1999 (Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 7 Sayı: 2
- Basım Tarihi: 1999
- Doi Numarası: 10.1177/021849239900700216
- Dergi Adı: Asian Cardiovascular and Thoracic Annals
- Derginin Tarandığı İndeksler: Scopus
- Sayfa Sayıları: ss.138-141
- İstanbul Yeni Yüzyıl Üniversitesi Adresli: Hayır
Özet
Rupture of an ascending aortic aneurysm is the most common cause of death in patients with Marfan syndrome, while type-A aortic dissection is the second most common fatal lesion. The aortic root dimension and the rate at which it increases are the best indications for surgical treatment. We regard aortic enlargement to 5.5 cm as the upper limit of safety, and we are inclined to advocate surgery at an earlier stage in high-risk families. We report our results of the surgical management of aortic aneurysm in the two siblings; a third sibling is currently being followed medically.