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Successful surgical repair of pulmonary dominant common arterial trunk without aortic arch obstruction in a neonate
Author(s) -
Harikrishnan Nair,
John Valliattu,
Raghavannair Suresh Kumar,
Robert H. Anderson,
Sajith Sulaiman,
Ashwin Varghese Alexander
Publication year - 2021
Publication title -
annals of pediatric cardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.292
H-Index - 19
eISSN - 0974-2069
pISSN - 0974-5149
DOI - 10.4103/apc.apc_239_20
Subject(s) - medicine , aortic arch , elephant trunks , trunk , cardiology , aortic arch syndrome , surgery , aorta , ecology , biology
The pulmonary dominant variant of the common arterial trunk has always been reported to be associated with aortic coarctation, or interruption of the aortic arch, along with a duct-dependent systemic circulation. This mandates a complex surgical repair with attendant high surgical mortality. We report a 23-day-old baby with a pulmonary dominant trunk with mild aortic hypoplasia but with an arch free of coarctation or interruption, who underwent successful surgical repair. In the preoperative evaluation of a common arterial trunk, pulmonary dominance may not necessarily denote an adverse risk factor when the aorta is only mildly hypoplastic.

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