# Benign to Malignant Hepatic Lesion Transformation in Abernethy Malformation

**Authors:** Chloe K. Tom, Ramon Ter-Oganesyan, Chopra Shefali, Navpreet Kaur, Jordan L. Pace, Ali Rastegarpour, Yuri Genyk, Jeffrey A. Kahn

PMC · DOI: 10.14309/crj.0000000000001307 · ACG Case Reports Journal · 2024-04-05

## TL;DR

This paper reports a rare case of a liver condition leading to the transformation of a benign tumor into a malignant one.

## Contribution

The novelty lies in documenting the progression from benign to malignant liver lesions in Abernethy malformation.

## Key findings

- Abernethy malformation can lead to focal nodular hyperplasia.
- The benign tumor progressed to hepatocellular carcinoma in the reported case.
- This case highlights the potential for malignant transformation in this rare condition.

## Abstract

Abernethy malformation or congenital extrahepatic portosystemic shunt is an extremely rare condition whereby the portomesenteric blood drains into a systemic vein and bypasses the liver through a complete or partial shunt. Severe complications include hyperammonemia and encephalopathy, benign and malignant liver tumors, and hepatopulmonary syndrome. We describe a case where a female adult diagnosed with congenital extrahepatic portosystemic shunt subsequently developed focal nodular hyperplasia and then hepatocellular carcinoma.

## Linked entities

- **Diseases:** encephalopathy (MONDO:0005560), hepatopulmonary syndrome (MONDO:0004694), focal nodular hyperplasia (MONDO:0100549), hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Diseases:** Hepatic Lesion (MESH:D056486), Benign (MESH:D009369), focal nodular hyperplasia (MESH:D020518), hepatopulmonary syndrome (MESH:D020065), liver tumors (MESH:D008113), Abernethy Malformation (MESH:C564254), hepatocellular carcinoma (MESH:D006528), encephalopathy (MESH:D001927), hyperammonemia (MESH:D022124)

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC10997230/full.md

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Source: https://tomesphere.com/paper/PMC10997230