A Case of Double Chambered Right Ventricle with Congenital Right Ventricular True Diverticulum
Korean Circulation Journal
; : 675-680, 1994.
Article
em Ko
| WPRIM
| ID: wpr-103606
Biblioteca responsável:
WPRO
ABSTRACT
Congenital diverticula of the cardiac ventricle have been reported as arising either from the left ventricule or, rarely from both ventricules. A diverticulum arising from the right ventricle alone is very rare. Double chambered right ventricle(DCRV) was first described in 1962 by Lucas et al, and account for 1.5% of congenital heart disease. Right ventricular diverticulum are associated with right ventricle outlet obstructive disease, tetralogy of fallot, double outlet right ventricle, pulmonic stenosis, ventricular septal defect, left ventricule-right atrium communication, persistant truncus arteriosus. DCRV are freqently associated with ventricular septal defect(80%), pulmonic stenosis(33%), renal anormaly(43%). Treatment consist of suture of diverticulum and resection of septum. We report a case of double chambered right ventricle with congenital right ventricular true diverticulum in 62 years of female patients admitted due to anterior chest pain and mild exertional dyspnea.
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Texto completo:
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Índice:
WPRIM
Assunto principal:
Estenose da Valva Pulmonar
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Suturas
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Tetralogia de Fallot
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Tronco Arterial
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Dor no Peito
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Dupla Via de Saída do Ventrículo Direito
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Divertículo
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Dispneia
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Cardiopatias Congênitas
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Comunicação Interventricular
Limite:
Female
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Humans
Idioma:
Ko
Revista:
Korean Circulation Journal
Ano de publicação:
1994
Tipo de documento:
Article