Peutz-Jeghers syndrome diagnostic study of choice: Difference between revisions
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The diagnosis of Peutz-Jeghers syndrome is made when at least 2 of the following 3 diagnostic criteria are met: | The diagnosis of Peutz-Jeghers syndrome is made when at least 2 of the following 3 diagnostic criteria are met: | ||
*Positive [[family history]] | *Positive [[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 | *[[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 usually the first lesions to appear and thus play an important part in the early diagnosis | ||
*Presence of [[hamartomatous]] [[polyps]] in the [[gastrointestinal tract]] | *Presence of [[hamartomatous]] [[polyps]] in the [[gastrointestinal tract]] | ||
Revision as of 20:42, 18 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
The diagnosis of Peutz-Jeghers syndrome is made when at least 2 of the following 3 diagnostic criteria are met: positive family history, mucocutaneous pigmentation, and presence of hamartomatous polyps.
Diagnostic Criteria
The diagnosis of Peutz-Jeghers syndrome is made when at least 2 of the following 3 diagnostic criteria are met:
- Positive 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 usually the first lesions to appear and thus play an important part in the early diagnosis
- Presence of hamartomatous polyps in the gastrointestinal tract