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Cardiol Young ; 33(11): 2446-2448, 2023 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-37492020

RESUMEN

An idiopathic enlargement of the right atrium is an extremely rare cardiac malformation. There are no established guidelines for the management of this disease, especially concerning medical versus surgical therapeutic approach and the timing for an operation. We report in this case about a neonate that first was treated conservatively until the age of 5 month and finally got an operative resection of the aneurysm. After surgery, unexpected complications occurred. A second aneurysm in the left atrium was demasked. Furthermore, a progressive dilatation of both atrial chambers after resection required regular follow-up and ongoing evaluation of treatment.


Asunto(s)
Aneurisma , Apéndice Atrial , Fibrilación Atrial , Aneurisma Cardíaco , Recién Nacido , Humanos , Atrios Cardíacos/anomalías , Aneurisma/complicaciones , Cardiomegalia/etiología , Aneurisma Cardíaco/diagnóstico por imagen , Aneurisma Cardíaco/cirugía
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