Hypervascular solid-appearing serous cystadenoma as a mimic of nonfunctioning pancreatic neuroendocrine tumour: a systematic review.

Abdom Radiol (NY)Apr 25, 2026 (epub)

Mario Annecchiarico, Giuseppe Loiaco, Giulio Argenio et al.

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In 30 seconds

This PRISMA-aligned systematic review examined solid-appearing serous cystadenomas (SCA) that can mimic nonfunctioning pancreatic neuroendocrine tumours (NF-pNET), synthesizing comparative imaging cohorts separately from case reports and series. It included 35 publications: four retrospective single-centre cohorts and 31 case reports or series. In the cohorts, unenhanced CT attenuation was consistently lower in SCA than NF-pNET (18.5-29.6 vs. 38.8-48.4 HU), while diffusion-weighted MRI showed higher ADC values in SCA. Arterial hyperenhancement and somatostatin-receptor imaging uptake were not specific for NF-pNET.

Key findings

  • Across comparative cohorts, unenhanced CT attenuation was 18.5-29.6 vs. 38.8-48.4 HU for SCA and NF-pNET, respectively.
  • Reported DWI-ADC cutoffs favoring SCA were > 1.36 × 10 - 3 mm 2 /s and > 1.99 × 10 - 3 mm 2 /s.
  • In case reports and series, arterial hyperenhancement occurred in 32/33 (97.0%) and 68 Ga-DOTA-peptide uptake in 17/39 (43.6%) of SCA cases.
  • EUS-guided sampling was diagnostic in 9/17 (52.9%) of reported cases.

Why it matters

A benign SCA mistaken for NF-pNET may lead to pancreatic resection. The review highlights imaging features that may help distinguish these lesions, while showing that hyperenhancement and positive somatostatin-receptor imaging can occur in SCA and therefore do not establish NF-pNET. Considering multiple imaging features may help avoid overreliance on a single suggestive finding.

What to keep in mind

Evidence came from retrospective single-centre comparative cohorts of resected, pathology-proven lesions and case reports or series; no meta-analysis was performed. The authors caution that proposed imaging thresholds lack external validation.

Source

Published in Abdom Radiol (NY). This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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