Paraganglioma Mimicking a Pancreatic Neoplasm

  • Nicole Lightfoot Department of Pathology, University of Melbourne, Austin Health. Heidelberg, VIC, Australia
  • Peter Santos Department of Nuclear Medicine, University of Melbourne, Austin Health. Heidelberg, VIC, Australia
  • Mehrdad Nikfarjam Department of Surgery, University of Melbourne, Austin Health. Heidelberg, VIC, Australia
Keywords: Neural Crest, Pancreas, Paraganglioma, Retroperitoneal Space

Abstract

Context Paragangliomas are rare tumours of neural crest origin. Extra-adrenal pancreatic paragangliomas are exceptionally rare. Case report A 66-year-old man with abdominal pain was noted to have a complex pancreatic head and uncinate process mass on imaging. He underwent complete resection by pancreaticoduodenectomy with final pathology confirming a 6 cm paraganglioma without evidence of metastases. On histology the tumour was arising from the retroperitoneum and abutting the pancreas. The patient was disease free at 14-month follow-up. Conclusion Pancreatic paragangliomas represent in many cases the retroperitoneal extension of a paraganglioma into the pancreas rather than a true pancreatic neoplasm. Although generally benign, the risk of malignant transformation justifies aggressive management.

Image: CT-PET showing no uptake within the cystic component of the mass.

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References

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CT-PET showing no uptake within the cystic component of the mass
Published
2011-05-06
How to Cite
LightfootN., SantosP., & NikfarjamM. (2011). Paraganglioma Mimicking a Pancreatic Neoplasm. JOP. Journal of the Pancreas, 12(3), 259-261. https://doi.org/10.6092/1590-8577/3293
Section
CASE REPORT