Affiliation:
1. Department of Cardiology, Dr. DY Patil Medical College Hospital and Research Centre, Pune, Maharashtra, India
Abstract
Aortopulmonary window (AP window) is an uncommon congenital heart condition marked by a connection between the ascending aorta and the pulmonary trunk. Numerous individuals diagnosed with AP window typically manifest symptoms in their early childhood, which may include recurring respiratory tract infections due to a left-to-right shunt, signs of congestive heart failure, and, if not treated in early childhood, the condition can progress to severe pulmonary vascular disease and Eisenmenger syndrome. Without treatment, very few patients survive beyond their second decade of life. In this case, we present a patient who exhibited symptoms of an ischemic stroke while having an undiagnosed large AP window and Eisenmenger syndrome.
Reference5 articles.
1. Aortopulmonary window in adulthood: Surviving at 22 years without intervention or pulmonary vascular disease;Yüksel;Turk Kardiyol Dern Ars,2016
2. Distal type of aortopulmonary window. Report of 4 cases;Mori;Br Heart J,1978
3. Diagnosis, treatment and outcomes of patients with aortopulmonary window;Demir;Balkan Med J,2013
4. A case of aortopulmonary window: Asymptomatic until the first pregnancy;Kose;Case Rep Cardiol,2015
5. Aortopulmonary window: Factors associated with early and late success after surgical treatment;van Son;Mayo Clin Proc,1993