# Isolated Gamma-Glutamyl Transferase Elevation in an Asymptomatic Adolescent: An Unusual Presentation of Focal Nodular Hyperplasia

**Authors:** Manuel Lima Ferreira, Teresa Cachada Baptista, Diana Alba, Ana Reis

PMC · DOI: 10.7759/cureus.88050 · 2025-07-16

## TL;DR

A 16-year-old girl with no symptoms had elevated GGT levels, leading to the discovery of a rare liver condition called focal nodular hyperplasia.

## Contribution

This case highlights isolated GGT elevation as a potential indicator of focal nodular hyperplasia in asymptomatic adolescents.

## Key findings

- The patient had persistent isolated gamma-glutamyl transferase elevation without symptoms.
- Imaging confirmed focal nodular hyperplasia despite the absence of a central scar.
- Conservative follow-up was chosen due to the asymptomatic nature of the condition.

## Abstract

Incidental liver lesions (ILLs) in children are increasingly being identified due to the widespread use of imaging techniques. Focal nodular hyperplasia (FNH) is relatively rare in pediatric age, typically diagnosed based on characteristic imaging findings. We report the case of a 16-year-old asymptomatic female patient with persistent isolated elevation of gamma-glutamyl transferase (GGT), identified during routine evaluation. Further imaging, including abdominal ultrasound and magnetic resonance imaging with hepatocyte-specific contrast agent, revealed an ILL consistent with FNH, despite the absence of a classical central scar. The adolescent remained asymptomatic, and conservative follow-up was decided. This case highlights the diagnostic relevance of isolated GGT elevation as a potential indicator of FNH.

## Linked entities

- **Diseases:** focal nodular hyperplasia (MONDO:0100549)

## Full-text entities

- **Genes:** GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}
- **Diseases:** FNH (MESH:D020518), ILLs (MESH:D008107)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12355200/full.md

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Source: https://tomesphere.com/paper/PMC12355200