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Abernethy malformation with unusual cardiac malformation: case report and literature review
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  • Liyuan Xu,
  • Hongju Zhang,
  • Guowen Liu,
  • Yunpeng Li,
  • Di Li,
  • Ning Ma
Liyuan Xu
Beijing Children's Hospital Capital Medical University

Corresponding Author:[email protected]

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Hongju Zhang
Beijing Children's Hospital Capital Medical University
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Guowen Liu
Beijing Children's Hospital Capital Medical University
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Yunpeng Li
Beijing Children's Hospital Capital Medical University
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Di Li
Capital Medical University Beijing Children's Hospital Imaging Centre
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Ning Ma
Beijing Children's Hospital Capital Medical University
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Abstract

Abernethy malformation, also known as congenital extrahepatic shunt, is a rare anomaly characterized by partial or complete diversion of the portal blood into the systemic venous circulation. The clinical manifestations of Abernethy malformation during childhood include neonatal cholestasis, failure to thrive, mental retardation, and other congenital defects. We report a case of Abernethy malformation Type Ⅱ in a 9-year-old boy whose left ventricle was slightly enlarged because of several major aortopulmonary collateral arteries but normal laboratory examinations five years earlier. The characteristics of congenital heart disease in patients with Abernethy malformation are discussed. We propose that enlargement of the left ventricular with systemic-pulmonary collateral circulation should raise the suspicion of Abernethy malformation.
14 Aug 2022Submitted to Echocardiography
16 Aug 2022Submission Checks Completed
16 Aug 2022Assigned to Editor
20 Aug 2022Reviewer(s) Assigned
16 Sep 2022Review(s) Completed, Editorial Evaluation Pending
17 Sep 2022Editorial Decision: Revise Major
28 Oct 20221st Revision Received
01 Nov 2022Submission Checks Completed
01 Nov 2022Assigned to Editor
02 Nov 2022Reviewer(s) Assigned
12 Nov 2022Review(s) Completed, Editorial Evaluation Pending
20 Nov 2022Editorial Decision: Accept
14 Dec 2022Published in Echocardiography. 10.1111/echo.15504