İleri Yaşta Tanı Alan Doğuştan Düzeltilmiş Büyük Arterlerin Transpozisyonu ve Situs İnversus Totalis Vakası
Abstract
Congenitally corrected transposition of the great arteries is a rare congenital anomaly, that is usually diagnosed in childhood or early adulthood. There are case reports of newly diagnosed patients at their 60’s in the literature. Our patient is a 72 year old male, complaining of worsening shortness of breath and heart failure symptoms for a year. He had the recent diagnosis of corrected transposition at his admission.
Keywords
Congenitally Corrected Transposition of Great Arteries, L-type Transposition, Situs Inversus Totalis
References
- 1. Ferencz C, Rubin JD, McCarter RJ et al. Congenital heart disease: Prevalence at live birth. Am J Epidemiol 1985;121:31-36.
- 2. Wallis GA, Debich-Spicer D, Anderson RH. Congenitally corrected transposition. Orphanet Journal of Rare Diseases 2011; 6:22-34
- 3. Carole A. Warnes. Transposition of the Great Arteries. Circulation 2006; 114: 2699-2709.
- 4. Cardell LS. Corrected transposition of the great vessels. Br Heart J 1956, 18:186.
- 5. Shapiro EP, Rademakers FE: Importance of oblique fiber orientation for left ventricular wall deformation. Technol Health Care 1997; 5:21-28.
- 6. Oliver JM, Gallego P, Gonzalez AE et al. Comparison of outcomes in adults with congenitally corrected transposition with situs inversus versus situs solitus. Am J Cardiol. 2012;110:1687-1691.
- 7. Koželj M, Cviji M, Berden P et al. A 6- year follow-up study of adult patients with congenitally corrected transposition. Cardiol Young. 2014;19:1-8.