Peutz-Jeghers syndrome

Peutz-Jeghers syndrome 

Updated: 01/10/2023

© Jun Wang, MD, PhD

General features
  • Autosomal dominant with variable penetrance, usually diagnosed in 20’s
  • Markedly increased risk of malignancies of different organs, including gastric type adenocarcinoma of cervix
  • May have Sertoli cell tumor of ovary
Genetic abnormalities
  • STK-11
Diagnostic criteria
  • 3+ histologically confirmed Peutz-Jeghers polyps
  • Any Peutz-Jeghers polyp with a family history
  • Characteristic melanotic mucocutaneous pigmentation (lips, oral mucosa, genitalia, digits, palms and soles) with a family history
  • Peutz-Jegher polyp and characteristic mucocutaneous pigmentation
Peutz-Jeghers polyp



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