Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Peutz-Jeghers syndrome}} | {{Peutz-Jeghers syndrome}} | ||
{{CMG}} {{AE}} {{HQ}} | {{CMG}}; {{AE}} {{HQ}} | ||
==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]], [[juvenile polyposis]], [[Addison's disease]], and [[McCune-Albright syndrome]]. | 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]]. | ||
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*[[Bannayan–Riley–Ruvalcaba syndrome]] | *[[Bannayan–Riley–Ruvalcaba syndrome]] | ||
*[[Juvenile polyposis]] | *[[Juvenile polyposis]] | ||
*[[McCune-Albright syndrome]] | *[[McCune-Albright syndrome]] | ||
Revision as of 16:45, 20 December 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [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
- McCune-Albright syndrome
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References
- ↑ Buck, J L; Harned, R K; Lichtenstein, J E; Sobin, L H (1992). "Peutz-Jeghers syndrome". RadioGraphics. 12 (2): 365–378. doi:10.1148/radiographics.12.2.1561426. ISSN 0271-5333.