Pancreatic Neuroendocrine Tumors: Computed Tomography Enhancement, but Not Histological Grade, Correlates with Tumor Aggression

Motoyo Yano, Sunil Misra, Danielle H. Carpenter, Amber Salter, Charles F. Hildebolt

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Objectives The aims of this study were to assess computed tomography enhancement of pancreatic neuroendocrine tumors (NETs), determine correlation with histological vascularity and fibrosis, and identify a biomarker for tumor aggression. Methods The arterial and venous enhancement of NET was calculated on computed tomography for 56 patients. Tumor size and vascularity/fibrosis were assessed. Tumor aggression was grouped by World Health Organization and Hochwald grade and the presence of metastases. Variables were assessed for correlation. Groups were compared using t test/Wilcoxon rank sum test. Results Arterial enhancement and dynamic washout (r = 0.35, P = 0.02; r = 0.34, P = 0.02, respectively) correlate with vascularity. There is inverse correlation between vascularity and fibrosis (r = -0.62, P < 0.001), but no correlation between enhancement and fibrosis. Metastatic NET had less arterial (mean, -2 [standard deviationi {SD}, 27.1] Hounsfield unit [HU]; 35.7 [SD, 57.5] HU; P = 0.01) and venous (12.6 [SD, 14.4] HU; 29.2 [SD, 38.3] HU; P = 0.04) enhancement and less washout (8.5 [SD, 18.5] HU; 26.8 [SD, 30] HU, P = 0.02) compared with nonmetastatic NET. These differences were not present when comparing by tumor grade. Arterial hypoenhancement was the only significant predictor of metastases. Conclusions Aggressive tumors, as determined by metastases, but not histological grade, enhance less than nonmetastatic tumors.

Original languageEnglish (US)
Pages (from-to)1366-1372
Number of pages7
JournalPancreas
Volume46
Issue number10
DOIs
StatePublished - Nov 1 2017
Externally publishedYes

Keywords

  • bioimaging
  • computed tomography
  • fibrosis
  • neoplasm metastases
  • neuroendocrine tumor
  • pancreas

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Hepatology
  • Endocrinology

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