• MEN1: the number “1” in MEN1 should remind you of primary or prime number. MEN1 involves things that start with the letter P:
    • Pituitary adenoma
    • Parathyroid hyperplasia
    • Pancreatic islet cell tumors (gastrinoma, insulinoma, glucagonoma)
  • MEN2A: happens to involve the letter C (This is MEN2A, so there are two C’s in each item!):
    • Calcitonin (medullary carcinoma of the thyroid with elevated calcitonin level)
    • Calcium (parathyroid hyperplasia, which causes elevated calcium levels)
    • Catecholamines which are made in the chromocytes (as in pheochromocytoma)
  • Men 2B: B is for big (marfanoid habitus) and for belly problems (mucosal neuromas)
  • MEN 1
    • Mutation of the MEN1 gene (located on chromosome 11) → altered expression of menin protein
  • MEN 2
    • Altered expression of the RET proto-oncogene → elevated tyrosine kinase activity
    • MEN 2B
  • See Hereditary cancer syndromes