Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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==Differentiating Peutz-Jeghers Syndrome from other Diseases== | ==Differentiating Peutz-Jeghers Syndrome from other Diseases== | ||
Peutz-Jeghers syndrome must be differentiated from the following diseases:<ref | Peutz-Jeghers syndrome must be differentiated from the following diseases:<ref>{{Pathology of Peutz-Jeghers syndrome. Dr Amir Rezaee and Dr Alexandra Stanislavsky et al. Radiopaedia.org 2015. http://radiopaedia.org/articles/peutz-jeghers-syndrome-2}}</ref> | ||
*[[Cowden syndrome]] | *[[Cowden syndrome]] | ||
*Cronkhite-Canada syndrome | *Cronkhite-Canada syndrome | ||
Revision as of 17:21, 24 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, juvenile polyposis, Addison's disease, and McCune-Albright syndrome.
Differentiating Peutz-Jeghers Syndrome from other Diseases
Peutz-Jeghers syndrome must be differentiated from the following diseases:[1]
- Cowden syndrome
- Cronkhite-Canada syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- Juvenile polyposis
- Addison's disease
- McCune-Albright syndrome