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An echocardiographic finding mimicking tricuspid atresia in a neonate with dilated cardiomyopathy

Part of: Echocardiography

Published online by Cambridge University Press:  05 August 2021

Daiji Takajo Open the ORCID record for Daiji Takajo [Opens in a new window] ,
Pooja Gupta  and
Sanjeev Aggarwal
Daiji Takajo*
Affiliation:
Division of Pediatric Cardiology, Department of Pediatrics, Children’s Hospital of Michigan, Detroit, Central Michigan University, Detroit, MI, USA
Pooja Gupta
Affiliation:
Division of Pediatric Cardiology, Department of Pediatrics, Children’s Hospital of Michigan, Detroit, Central Michigan University, Detroit, MI, USA
Sanjeev Aggarwal
Affiliation:
Division of Pediatric Cardiology, Department of Pediatrics, Children’s Hospital of Michigan, Detroit, Central Michigan University, Detroit, MI, USA
*
Author for correspondence: Daiji Takajo, Division of Pediatric Cardiology, Department of Pediatrics, Children’s Hospital of Michigan, 3901 Beaubien Boulevard, Detroit, MI 48201, USA. Tel: +1 (313) 745–1892; Fax: (313) 993–7118. E-mail: dt1449@gmail.com
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Abstract

We report a neonate with dilated cardiomyopathy and have echocardiographic findings consistent with “functional” tricuspid atresia. There was an echo-bright, plate-like tissue at the tricuspid valve position with no forward flow across it. This report underscores the role of right ventricle intracavitary haemodynamic influence on the tricuspid valve leaflet excursion and demonstrates a phenomenon of “pseudo or functional tricuspid atresia” mimicking tricuspid atresia in a patient with acute presentation of cardiomyopathy.

Keywords

Functional tricuspid atresiacardiomyopathyBarth syndrome
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 3 , March 2022 , pp. 497 - 499
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Copyright
© The Author(s), 2021. Published by Cambridge University Press

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References

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