Well-differentiated Pancreatic Neuroendocrine Tumor in a Patient with Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM)

Michaël Noë, Wenzel M. Hackeng, Wendy W.J. De Leng, Menno Vergeer, Frank P. Vleggaar, Folkert H.M. Morsink, Laura D. Wood, Ralph H. Hruban, G. Johan A. Offerhaus, Lodewijk A.A. Brosens

Research output: Contribution to journalArticle

Abstract

Germline mutations in CDKN2A result in Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM), which is associated with an increased risk for pancreatic ductal adenocarcinoma and melanoma. CDKN2A is somatically inactivated in multiple neoplasms, raising the possibility that, although the data are not conclusive, germline CDKN2A mutation may also impose an increased risk for other neoplasms. We present a patient with a CDKN2A germline mutation (p16-Leiden mutation) and mosaicism for neurofibromatosis type 2, who presented with a small asymptomatic pancreatic lesion, detected during endoscopic ultrasound screening of the pancreas. After resection, the lesion was found to be a well-differentiated pancreatic neuroendocrine tumor (PanNET). Molecular analysis of the tumor showed somatic loss of the second allele, supporting a causal relation of the PanNET to the underlying FAMMM syndrome. Recent data, showing the association between certain single-nucleotide polymorphisms in the CDKN2A gene and an increased incidence for PanNET, further support a role for germline CDKN2A alterations in PanNET risk. We conclude that PanNETs can be a phenotypic expression of FAMMM syndrome. This can have implications for screening and for the diagnosis of pancreatic neoplasms in carriers of germline CDKN2A mutations.

Original languageEnglish (US)
Pages (from-to)1297-1302
Number of pages6
JournalAmerican Journal of Surgical Pathology
Volume43
Issue number9
DOIs
StatePublished - Sep 1 2019

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Keywords

  • CDKN2A
  • P16
  • cancer
  • cancer syndrome
  • early detection
  • molecular pathology
  • neuroendocrine tumor
  • pancreas

ASJC Scopus subject areas

  • Anatomy
  • Surgery
  • Pathology and Forensic Medicine

Cite this

Noë, M., Hackeng, W. M., De Leng, W. W. J., Vergeer, M., Vleggaar, F. P., Morsink, F. H. M., Wood, L. D., Hruban, R. H., Offerhaus, G. J. A., & Brosens, L. A. A. (2019). Well-differentiated Pancreatic Neuroendocrine Tumor in a Patient with Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM). American Journal of Surgical Pathology, 43(9), 1297-1302. https://doi.org/10.1097/PAS.0000000000001314