Canadian Journal of Gastroenterology (Jan 1988)

Peutz-Jeghers Syndrome without Polyposis

  • Anthony G. Catto-Smith,
  • Mark K. Patrick,
  • D. Grant Gall

DOI
https://doi.org/10.1155/1988/451742
Journal volume & issue
Vol. 2, no. 3
pp. 117 – 118

Abstract

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Peutz-Jeghers syndrome is generally considered a condition in which familial gastrointestinal polyposis is associated with a characteristic pigmentation of the skin and mucous membranes Two members of a family in which the characteristic pigmentation was present in the absence of gastrointestinal polyposis arc reported. These patients highlight the importance of defining the intestinal lesion associated with this syndrome.