مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

PEUTZ-JEGHERS SYNDROME WITHOUT MUCOCUTANEOUS PIGMENTATION: A CASE REPORT

Pages

  169-173

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.

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  • Cite

    APA: Copy

    MOZAFFAR, MOHAMMAD, SOBHIYEH, MOHAMMAD REZA, HASANI, MOHAMMAD, & FALLAH, MAHTAB. (2012). PEUTZ-JEGHERS SYNDROME WITHOUT MUCOCUTANEOUS PIGMENTATION: A CASE REPORT. GASTROENTEROLOGY AND HEPATOLOGY FROM BED TO BENCH, 5(3), 169-173. SID. https://sid.ir/paper/324548/en

    Vancouver: Copy

    MOZAFFAR MOHAMMAD, SOBHIYEH MOHAMMAD REZA, HASANI MOHAMMAD, FALLAH MAHTAB. PEUTZ-JEGHERS SYNDROME WITHOUT MUCOCUTANEOUS PIGMENTATION: A CASE REPORT. GASTROENTEROLOGY AND HEPATOLOGY FROM BED TO BENCH[Internet]. 2012;5(3):169-173. Available from: https://sid.ir/paper/324548/en

    IEEE: Copy

    MOHAMMAD MOZAFFAR, MOHAMMAD REZA SOBHIYEH, MOHAMMAD HASANI, and MAHTAB FALLAH, “PEUTZ-JEGHERS SYNDROME WITHOUT MUCOCUTANEOUS PIGMENTATION: A CASE REPORT,” GASTROENTEROLOGY AND HEPATOLOGY FROM BED TO BENCH, vol. 5, no. 3, pp. 169–173, 2012, [Online]. Available: https://sid.ir/paper/324548/en

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