Cardiac rhabdomyoma mimicking haemodynamics of hypoplastic left heart syndrome.
Acta Cardiol
; 69(3): 308-10, 2014 Jun.
Article
em En
| MEDLINE
| ID: mdl-25029876
ABSTRACT
Cardiac rhabdomyomas are rare and often regress spontaneously. However, the management of rhabdomyoma with severe inflow and outflow obstructions is a challenge. An infant with a massive left ventricular rhabdomyoma mimicking the haemodynamics of hypoplastic left heart syndrome is reported. Surgery could not be contemplated because the mitral valve leaflets and chordae were imbedded in the tumour mass. The arterial duct (AD) was kept open to perfuse the systemic circulation and palliations with pulmonary artery branch banding and AD stenting were planned. However; while waiting for spontaneous regression of the tumour, the child died of circulatory collapse when 4 weeks old.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Rabdomioma
/
Síndrome do Coração Esquerdo Hipoplásico
/
Hemodinâmica
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
Limite:
Humans
/
Male
/
Newborn
Idioma:
En
Revista:
Acta Cardiol
Ano de publicação:
2014
Tipo de documento:
Article