Peutz-Jeghers syndrome diagnostic study of choice: Difference between revisions

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==Overview==
==Overview==
Peutz-Jeghers syndrome is diagnosed if the patient presented with two of the three major clinical criterions (family history, mucocutaneous pigmentation, and hamartomatous polyps)
Peutz-Jeghers syndrome is diagnosed if the patient presented with two of the three major clinical criterions (family history, mucocutaneous pigmentation, and hamartomatous polyps)
==Diagnostic Criteria==
==Diagnostic Criteria==
Peutz-Jeghers syndrome is diagnosed if the patient presented with two of the following three major clinical criterions:
Peutz-Jeghers syndrome is diagnosed if the patient presented with two of the following three major clinical criterions:
*Family history
*[[Family history]]
*Mucocutaneous pigmentation causing patches of hyperpigmentation in the oral mucosa ([[gingiva]], [[hard palate]], [[buccal mucosa]], and labial mucosa) and on the hands and feet. The oral pigmentations are the first on the body to appear, and thus play an important part in early diagnosis
*[[Mucocutaneous]] [[pigmentation]] causing patches of hyperpigmentation in the oral mucosa ([[gingiva]], [[hard palate]], [[buccal mucosa]], and labial mucosa) and on the hands and feet. The oral pigmentations are the first on the body to appear, and thus play an important part in early diagnosis
*Hamartomatous polyps in the gastrointestinal tract
*[[Hamartomatous]] [[polyps]] in the [[gastrointestinal tract]]

Revision as of 13:19, 10 September 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Mohamad Alkateb, MBBCh [2]

Overview

Peutz-Jeghers syndrome is diagnosed if the patient presented with two of the three major clinical criterions (family history, mucocutaneous pigmentation, and hamartomatous polyps)

Diagnostic Criteria

Peutz-Jeghers syndrome is diagnosed if the patient presented with two of the following three major clinical criterions: