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CASE REPORT
Neuroendocrine tumour in pancreatic dorsal agenesis: a rare association
  1. Pedro Rodrigues1,
  2. Rui Caetano Oliveira2,
  3. Carlos Miguel Oliveira1,
  4. Maria Augusta Cipriano1
  1. 1Pathology, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal
  2. 2Pathology, Hospitais da Universidade de Coimbra, Coimbra, Portugal
  1. Correspondence to Dr Rui Caetano Oliveira, ruipedrocoliveira{at}hotmail.com

Summary

Pancreatic dorsal agenesis (PDA) is a rare congenital anomaly, usually asymptomatic, that can present with abdominal pain, pancreatitis, diabetes mellitus and jaundice. Pancreatic tumours in PDA background are extremely rare, and when they occur are mainly pancreatic ductal adenocarcinoma. We present a case of a 48-year-old female patient with incidental detection of a 26×20 mm nodular lesion of the cephalic pancreas on ultrasound. Surgery was performed and gross examination revealed PDA with a tumour developed around the Wirsung duct. Histology showed a neuroendocrine tumour G1 with neural and vascular invasion. Two and half years later, the patient is alive and without tumour relapse. Awareness of the association of PDA and pancreatic tumours is fundamental in order to develop personalised follow-up programmes.

  • pancreas and biliary tract
  • pancreatic cancer
  • pathology

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Footnotes

  • Contributors PR and RCO collected clinical data, analysed the histopathology and performed the draft of the manuscript. CMO performed radiology examination. MAC helped with the histopathological analysis and reviewed critically the article for important intellectual content. All authors read and approved the final version of the manuscript.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.