ReviewAnnals of pediatric cardiology
Abernethy malformation: Our experience from a tertiary cardiac care center and review of literature.
Review in Annals of pediatric cardiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed.
- Development of Hepatocellular Carcinoma in Type IB Abernethy Malformation.ACG case reports journal · 2026Article
- Endovascular closure of a large intrahepatic portosystemic shunt in a three-month-old infant: a case report and literature review.Frontiers in pediatrics · 2026Article
- Developmental Anomalies of the Inferior Vena Cava and its Tributaries: What the Radiologist Needs to Know?The Indian journal of radiology & imaging · 2022Review
- Abernethy malformation: A comprehensive review.Diagnostic and interventional radiology (Ankara, Turkey) · 2022Review
- Case report: Congenital extrahepatic portocaval shunt presenting as pulmonary arterial hypertension in a pregnant patient.Pulmonary circulation · 2022Article
- How I do it: Novel technique to "Unmask" and treat congenital portosystemic venous connections in congenital heart disease.Annals of pediatric cardiologyArticle
- The physiological implications of absent ductus venosus during fetal and post-natal life.Annals of pediatric cardiologyArticle
- Congenital extrahepatic portocaval malformation: Rare but potentially treatable cause of pulmonary hypertension.Indian heart journalArticle
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Abernethy malformation, also called as congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Although rare, it is increasingly being reported and is important to diagnose given the adverse clinical consequences in untreated patients. It has myriad of clinical presentations, from being completely asymptomatic to causing hepatic carcinoma, hepatic encephalopathy, severe pulmonary hypertension, and diffuse pulmonary arteriovenous malformation. We describe our experience with five cases in a tertiary pediatric cardiac care center with Abernethy malformation, with review of literature and also discuss possible therapeutic implications.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.