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Table 4 Mutations in pancreatic MEN1 syndrome associated microadenomas and PanNETs, sporadic PanNETs and PanNECs

From: Surgical and molecular pathology of pancreatic neoplasms

Neoplasm

Mutations

MEN1

ATRX/DAXX

mTOR pathway

KRAS

TP53

RB1

MEN1 syndrome microadenomas

Up to 100 %

0 %

u

u

u

u

MEN-1 syndrome tumors

Up to 100 %

6 %

u

u

u

u

G1/G2 Pancreatic neuroendocrine tumors

45 %

45 %

15 %

0 %

0 %

0 %

G3 Pancreatic neuroendocrine carcinomas

u

0 %

u

30 %

60 %

70 %

  1. u unknown