Multiple endocrine neoplasia (MEN) is a collection of inherited syndrome associated with cancer
MEN 1- menin gene, MEN 2- RET gene
Men 1a (PPP)- parathyroid, pituitary, pancreatic (commonly gastrinomas or insulinomas) cancers
Men 2a (TPP)- thyroid, parathyroid, phaeochromocytoma cancers
Men 2b (TPN)- thyroid, phaeochromocytoma, neuroma cancers
Autosomal dominant: MEN 1, 2a & 2b
RET gene = rearranged during transfection
In children with parents who have MEN and moderate risk RET- screen for parathyroid cancer from the age of 5.
All cases of medullary thyroid cancer are tested for MEN RET mutation.
Rare cancers knowledgebase - multiple endocrine neoplasia syndromes (mens) (no date) Rare Cancers Australia Knowledge - Home. Available at: https://knowledge.rarecancers.org.au/knowledgebase/cancer-types/199/multiple-endocrine-neoplasia-syndromes (Accessed: 05 October 2024).
https://www.cancer.gov/publications/dictionaries/cancer-terms/def/men2a-syndrome
Page written in 2024.