Publisher: Research Institute for Gastroenterology and Liver Diseases (RIGLD)
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  3. Vol. 5 No. 3 (2012): Summer
  4. Case Report

ISSN: 2008-2258

Summer
Vol. 5 No. 3 (2012)

Peutz-Jeghers syndrome without mucocutaneous pigmentation: a case report

  • Mohammad Mozaffar
  • Mohammadreza Sobhiyeh
  • Mohammad hasani
  • Mahtab Fallah

Gastroenterology and Hepatology from Bed to Bench, Vol. 5 No. 3 (2012),
https://doi.org/10.22037/ghfbb.v5i3.283 Published 1 July 2012

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Abstract

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.

Keywords:
  • Hamartomatous polyps
  • Mucocutaneous pigmentations
  • Peutz-Jeghers syndrome
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How to Cite

Mozaffar, M., Sobhiyeh, M., hasani, M., & Fallah, M. (2012). Peutz-Jeghers syndrome without mucocutaneous pigmentation: a case report. Gastroenterology and Hepatology from Bed to Bench, 5(3). https://doi.org/10.22037/ghfbb.v5i3.283
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GHFBB journal is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).

Print ISSN: 2008-2258
Online ISSN: 2008-4234

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