Peutz-Jeghers syndrome differential diagnosis
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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][2]
- Cowden syndrome
- Cronkhite-Canada syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- Juvenile polyposis
- McCune-Albright syndrome
Differential diagnosis according to polys:
Diseases | History and Symptoms | Physical Examination | Laboratory Findings | Other Findings | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Abdominal Pain | Rectal Bleeding | Hyperpigmentation | Fatigue | Abdominal Tenderness | Hyperpigmentation | Anemia | Gene(s) | Sertoli Cell Tumors | Gastrointestinal Tumors | Cancers | ||
Juvenile Polyposis Syndrome | + | - | + | - | - | - | SMAD4 | - | Adenoma+
Hamartoma+++ |
Colon | ||
Cowden Syndrome | - | - | Axillary+ | - | - | Axillary+ | - | PTEN | - | Adenoma+
Hamartoma+++ |
Breast, Thyroid, Endometrium | Trichilemmoma, skin hamartoma, hyperplastic polyps, macrocephaly, breast fibrosis |
Carney Syndrome | - | - | Facial+ | - | - | Facial+ | - | PRKAR1A | ++ | Thyroid | Myxomas of skin and heart | |
Familial Adenomatous Polyposis | + | + | - | + | +/- | - | + | APC | - | Adenoma+++ | Colon, brain | Desmoid tumors, osteomas |
Hereditary Non-Polyposis Colon Cancer | - | + | - | + | +/- | - | + | MLH1 | - | Adenoma+ | Endometrial, gastric, renal pelvis, ureter, and ovarian | Sebaceous adenoma |
|
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.
- ↑ "Peutz-Jeghers Syndrome - GeneReviews® - NCBI Bookshelf".