Tricuspid valve dysplasia, other than Ebstein's anomaly, is a very rare congenital heart defect. During the prenatal and/or the neonatal periods the clinical picture is very critical. We here report on a newborn infant with severe tricuspid valve dysplasia and 4/4 tricuspid regurgitation, giant right atriomegaly, functional pulmonary atresia with ductal-dependent pulmonary blood flow. The child was successfully submitted to implantation of a 15 mm pulmonary stentless heterograft valve using the top-hat technique.

Surgical treatment of tricuspid valve dysplasia in the neonatal period / Butera, G.; Pome, G.; Giamberti, A.; Frigiola, A.; Chessa, M.; Carminati, M.. - In: ITALIAN HEART JOURNAL. - ISSN 1129-471X. - 4:3(2003), pp. 211-213.

Surgical treatment of tricuspid valve dysplasia in the neonatal period

Chessa M.
Conceptualization
;
Carminati M.
2003-01-01

Abstract

Tricuspid valve dysplasia, other than Ebstein's anomaly, is a very rare congenital heart defect. During the prenatal and/or the neonatal periods the clinical picture is very critical. We here report on a newborn infant with severe tricuspid valve dysplasia and 4/4 tricuspid regurgitation, giant right atriomegaly, functional pulmonary atresia with ductal-dependent pulmonary blood flow. The child was successfully submitted to implantation of a 15 mm pulmonary stentless heterograft valve using the top-hat technique.
2003
Pediatric cardiosurgery
Tricuspid valve
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/163938
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