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Cronkhite-Canada syndrome


  • not inherited; no pattern
  • inflammatory glandular dilatation of stomach, colon, SB (50%)
  • juvenile-type polyps

  • no malignant potential
  • protein and electrolyte loss
  • ectodermal abnormalities
    • alopecia
    • hyperpigmentation
    • nail loss (onycholysis)

  • prognosis:
    • males: remits
    • females: die in 6-18 months d/t cachexia

see: polyposis syndromes


Charles E. Kahn, Jr., MD  -  2 February 1995
Last updated:  1 October 2013


 

Related CHORUS documents:
polyposis syndromes
gastric polyps
Peutz-Jeghers syndrome
hyperplastic gastric polyp
Cowden syndrome
juvenile polyposis coli

 

Copyright © 2013, Charles E. Kahn, Jr.