Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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*[[Cowden syndrome]] | *[[Cowden syndrome]] | ||
*[[Bannayan–Riley–Ruvalcaba syndrome]] | *[[Bannayan–Riley–Ruvalcaba syndrome]] | ||
*[[Juvenile polyposis]] | *[[Juvenile polyposis]] | ||
*[[Addison's disease]] | |||
*[[McCune-Albright syndrome]] | |||
== References == | == References == | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 13:27, 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 must be differentiated from other diseases that cause hamartomatous polyps and mucocutaneous pigmentation, such as Cowden syndrome, Bannayan–Riley–Ruvalcaba syndrome, and juvenile polyposis.
Differentiating Peutz-Jeghers Syndrome from other Diseases
Peutz-Jeghers syndrome must be differentiated from the following diseases:
- Cowden syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- Juvenile polyposis
- Addison's disease
- McCune-Albright syndrome