Table 1.
Disease | Histological type | Gene mutation | Location | Incidence of thyroid cancer | Pathological variant of PTC |
---|---|---|---|---|---|
FAP and Gardner syndrome | PTC | APC tumor suppressor gene | 5q21 | 2–12% | Cribriform-morular classical variant |
Cowden syndrome | FTC, PTC, C-cell hyperplasia | PTEN tumor suppressor gene | 10q23.2 | >10% | |
Carney complex | FTC, PTC | PRKAR1-x | 2p16 17q22–24 | 60 and 4% | |
Werner syndrome | FTC, PTC, ATC | WRN gene | 8p11–p12 | 18% |
PTC, papillary thyroid cancer; FAP, familial adenomatous polyposis; APC, adenomatous polyposis coli; FTC, follicular thyroid cancer; PTEN, phosphatase and tensin; PRKAR1-x protein kinase A regulatory subunit type 1-alpha; ATC, anaplastic thyroid cancer; WRN, Werner.