# Liver Transplantation as a Treatment for Unresectable Hepatic Adenoma in a Patient With Abernethy Syndrome

**Authors:** Shreeja Patel, Dane Thompson, Mohamed Sharshar, James M Crawford, Nabil Dagher, Ahmed E Fahmy

PMC · DOI: 10.7759/cureus.60683 · Cureus · 2024-05-20

## TL;DR

This paper presents the first case of liver transplantation for a patient with Abernethy syndrome and a large, unresectable hepatic adenoma.

## Contribution

The paper reports the first use of deceased donor liver transplantation for Abernethy syndrome with unresectable hepatic adenoma.

## Key findings

- The patient had type 1 Abernethy syndrome with large hepatic adenomas that were confirmed to have focal hepatocellular carcinoma.
- Liver transplantation was performed successfully at age 41 after resection was deemed infeasible.
- The case highlights liver transplantation as a viable treatment for this rare and complex condition.

## Abstract

Abernethy syndrome is a rare congenital anomaly characterized by an intrahepatic or extrahepatic portosystemic shunt. Most patients are asymptomatic; however, due to the alteration in, or lack of, a portovenous flow, patients with Abernethy syndrome are at high risk of developing sequelae of liver failure. Once these complications develop, the only definitive treatment is transplantation. Patients with Abernethy syndrome are also at a higher risk of developing benign and malignant liver lesions, including hepatic adenomas. Here, we describe the first case of deceased donor liver transplantation as a treatment for a patient with type 1 Abernethy syndrome complicated by large, unresectable hepatic adenoma, found to have focal hepatocellular carcinoma on pathologic examination. Our male patient was found to have elevated liver enzymes at age 33, during a routine outpatient medical appointment. Despite being asymptomatic, his history of prior liver resection prompted CT imaging, which revealed two large liver lesions concerning for hepatic adenomas. When surveillance imaging showed a significant growth of the liver lesions, biopsy was pursued, which confirmed a diagnosis of hepatic adenomas. However, given the size of these lesions, resection was not a viable option for the patient. Instead, the patient underwent liver transplantation at age 41, which he tolerated well. Our case demonstrates the utility of deceased donor liver transplantation as a treatment for patients with Abernethy syndrome complicated by unresectable adenomas.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), liver failure (MONDO:0100192)

## Full-text entities

- **Diseases:** adenomas (MESH:D000236), liver failure (MESH:D017093), type 1 Abernethy syndrome (MESH:D003922), Abernethy Syndrome (MESH:D013577), liver lesions (MESH:D008107), hepatocellular carcinoma (MESH:D006528), Hepatic Adenoma (MESH:C564190), congenital anomaly (MESH:D000013)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11187450/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC11187450/full.md

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Source: https://tomesphere.com/paper/PMC11187450