# Clinical Value of ¹⁸F-fluorodeoxyglucose Positron Emission Tomography/Computed Tomography in Neuroendocrine Neoplasms: A Case Report and Literature Review

**Authors:** David Gutierrez Albenda, Mariana Parra, Ana María Gutiérrez, Ian Taylor, Gabriel Infante

PMC · DOI: 10.7759/cureus.103838 · 2026-02-18

## TL;DR

This paper discusses how ¹⁸F-FDG PET/CT can provide valuable insights into the progression of neuroendocrine tumors beyond traditional imaging methods.

## Contribution

The paper introduces the clinical value of ¹⁸F-FDG PET/CT in detecting aggressive tumor behavior in low-grade neuroendocrine neoplasms.

## Key findings

- ¹⁸F-FDG PET/CT revealed hypermetabolic nodal conglomerates not evident on SSR-based imaging.
- The imaging method identified heterogeneous metabolic behavior and possible tumor dedifferentiation.
- ¹⁸F-FDG PET/CT offers prognostic information beyond histological grading in low-grade NENs.

## Abstract

Neuroendocrine neoplasms (NENs) are rare and heterogeneous tumors in which functional imaging plays a central role in diagnosis, staging, and prognostic stratification. While somatostatin receptor (SSRs)-based imaging remains the standard for well-differentiated tumors, ¹⁸F-fluorodeoxyglucose (¹⁸F-FDG) positron emission tomography/computed tomography (PET/CT) provides complementary information on tumor metabolism and aggressiveness.
We present the case of a 52-year-old male diagnosed in 2013 with a low-grade pancreatic neuroendocrine tumor who underwent surgical resection followed by multiple reinterventions due to local progression and mesenteric metastases. Serial SSR PET/CT studies demonstrated high receptor expression in mesenteric lesions. However, subsequent ¹⁸F-FDG-PET/CT revealed a hypermetabolic mesenteric nodal conglomerate, suggesting heterogeneous metabolic behavior and possible tumor dedifferentiation.
This case highlights the clinical value of ¹⁸F-FDG-PET/CT in low-grade NENs, particularly for assessing disease progression, by providing prognostic information beyond histological grading alone. ¹⁸F-FDG-PET/CT may identify aggressive tumor components not evident on receptor-based imaging, supporting its role as a complementary tool in selected patients.

## Full-text entities

- **Diseases:** aggressiveness (MESH:D010554), NENs (MESH:D009369), metastases (MESH:D009362), pancreatic neuroendocrine tumor (MESH:D018358)
- **Chemicals:** 18F-FDG (MESH:D019788)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13004162/full.md

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Source: https://tomesphere.com/paper/PMC13004162