
An unusual combination of persistent silent truncus arteriosus Type-II with ascending aortic aneurysm
Author(s) -
Mohamed Farah Yusuf Mohamud,
Mohamed Abdullahi Mohamud,
Abdinafic Mohamud Hussein,
İsmail Gedi İbrahim
Publication year - 2020
Publication title -
journal of surgical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.14
H-Index - 3
ISSN - 2042-8812
DOI - 10.1093/jscr/rjaa216
Subject(s) - medicine , truncus arteriosus , ascending aorta , cardiology , truncus , aneurysm , aortic aneurysm , heart disease , aorta , surgery , tetralogy of fallot
Truncus arteriosus (TA) is a relatively uncommon cyanotic congenital cardiac anomaly accounting for 1.3% of all congenital cardiac malformations. TA associated with an ascending aortic aneurysm is an extremely rare congenital cardiovascular abnormality. A 15-year-old male presented with shortness of breath and cough for 2 weeks. Radiological examinations showed that the ascending aorta and main pulmonary arteries originate from a single truncus with ascending aortic aneurysm. TA has a poor prognosis if remain unrepaired and surgical intervention is necessary to avoid severe pulmonary vascular occlusive disease.
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