Aortopulmonary window and double aortic arch. A rare association
نویسندگان
چکیده
منابع مشابه
Aortopulmonary window and double aortic arch. A rare association.
We report the case of a 27-year-old male patient with dyspnea on physical exertion. Clinical assessment and various tests led to the diagnosis of aortopulmonary window and double aortic arch. According to a literature search, this may be the first report on such association.
متن کاملThree Cases of a Rare Association: Double Aortic Arch
Background Vascular ring is less than 1% of congenital heart disease. Double aortic arch (DAA) is the most common form of it. Its detecting is important because of the effects of pressure on the esophagus and trachea. Case Report In this study, three children suffering from double aortic arch with symptoms of dysphagia and recurrent aspiration, which in two cases had led to cardiac arrest, wer...
متن کاملthree cases of a rare association: double aortic arch
background vascular ring is less than 1% of congenital heart disease. double aortic arch (daa) is the most common form of it. its detecting is important because of the effects of pressure on the esophagus and trachea. case report in this study, three children suffering from double aortic arch with symptoms of dysphagia and recurrent aspiration, which in two cases had led to cardiac arrest, wer...
متن کاملAortopulmonary window and interrupted aortic arch in a neonate assessed by 64-slice computed tomography.
MOTS CLÉS Fenêtre A newborn baby, born prematurely at 34 weeks’ gestation, had a neonatal diagnosis of aortopulmonary window after respiratory distress at 6 days of life, with a systolic heart murmur. He underwent two-dimensional echocardiography, which depicted an 8mm defect between the aorta and the pulmonary artery with a massive left-to-right shunt (Fig. 1). Dual-source 64-channel multidete...
متن کاملCH D urgical management of aortopulmonary window ssociated with interrupted aortic arch : A Congenital Heart
esults: Interrupted aortic arch was type A in 17 patients and type B in 3 patients. ortopulmonary window morphology was type I (n 10), type II (n 5), and type II (n 5). Associated cardiovascular anomalies were common, including atrial eptal defect (n 13) and systemic venous anomalies (n 3). Overall survival after nitial admission was 91%, 86%, and 84% at 1, 5, and 10 years, respectively. Fiftee...
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ژورنال
عنوان ژورنال: Arquivos Brasileiros de Cardiologia
سال: 2001
ISSN: 0066-782X
DOI: 10.1590/s0066-782x2001001100009