Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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==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 | 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]], and [[McCune-Albright syndrome]]. | ||
==Differentiating Peutz-Jeghers Syndrome from other Diseases== | ==Differentiating Peutz-Jeghers Syndrome from other Diseases== | ||
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Revision as of 16:47, 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, 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.