Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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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]]. | 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== | ==Differentiating Peutz-Jeghers Syndrome from other Diseases== | ||
Peutz-Jeghers syndrome must be differentiated from: | Peutz-Jeghers syndrome must be differentiated from the following diseases: | ||
*Cowden syndrome | *[[Cowden syndrome]] | ||
*Bannayan–Riley–Ruvalcaba syndrome | *[[Bannayan–Riley–Ruvalcaba syndrome]] | ||
*juvenile polyposis | *[[juvenile polyposis]] | ||
== References == | == References == | ||
Revision as of 15:28, 9 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: