z-logo
open-access-imgOpen Access
Peutz-Jeghers syndrome without mucocutaneous pigmentation: a case report
Author(s) -
Mohammad Mozaffar,
Mohammad Reza Sobhiyeh,
Mohammad Hasani,
Mahtab Fallah
Publication year - 2012
Publication title -
gastroenterology and hepatology from bed to bench
Language(s) - English
DOI - 10.22037/ghfbb.v5i3.283
Peutz–Jeghers syndrome is a rare condition characterized by mucocutaneous pigmentation, polyposis and an increased cancer risk at a number of gastrointestinal and extra intestinal organs. We present a patient with a history of gastrointestinal bleeding with no mucocutaneous pigmentation. Upper and lower gastrointestinal endoscopy revealed multiple polyps located in the deuodenum and colon. Histopathological evaluation of the polyps revealed hamartomatous polyps of Peutz-Jeghers syndrome.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom