Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 4: | Line 4: | ||
==Overview== | ==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]]. | 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: | |||
*Cowden syndrome | |||
*Bannayan–Riley–Ruvalcaba syndrome | |||
*juvenile polyposis | |||
== References == | == References == |
Revision as of 15:25, 9 September 2015
Peutz-Jeghers syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Peutz-Jeghers syndrome differential diagnosis On the Web |
American Roentgen Ray Society Images of Peutz-Jeghers syndrome differential diagnosis |
Risk calculators and risk factors for Peutz-Jeghers syndrome differential diagnosis |
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:
- Cowden syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- juvenile polyposis