Peutz-Jeghers syndrome natural history, complications, and prognosis: Difference between revisions
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Revision as of 13:40, 14 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
If left untreated, patients with Peutz-Jeghers syndrome may progress to develop rectal bleeding, anemia, intussusception, bowel obstruction, and abdominal pain. Common complications of Peutz-Jeghers syndrome include colon cancer, and cachexia.[1] Prognosis is generally good if polypectomy was performed before any dysplastic degenerations take place.
Natural History
Without screening, patients with Peutz-Jeghers syndrome may develop symptoms of intestinal cancers (colon cancer) and extra intestinal cancers (e.g. pancreatic cancer and lung cancer), which will eventually lead to death.
Complications
Complications that can develop as a result of Peutz-Jeghers syndrome are:[2]
- Colon cancer
- Cachexia
- Anemia
- Intussusception
- GI tract adenocarcinoma, although the polyps themselves are not premalignant
- Extraintestinal malignancies:
- Adenoma malignum (adenocarcinoma subtype of cervix)
- Breast cancer
- Pancreatic cancer
- Ovaries: sex cord tumors
- Testis: Sertoli cell tumors
- Lung cancer
- Uterine cancer
Prognosis
Almost half of Peutz-Jeghers patients die from cancer by age 57 years, and the cumulative risk of developing a form of cancer associated with Peutz-Jeghers syndrome between ages 15-64 is 93%.[3]
References
- ↑ Zbuk KM, Eng C. Hamartomatous polyposis syndromes. Nat Clin Pract Gastroenterol Hepatol. 2007 Sep. 4(9):492-502.
- ↑ http://radiopaedia.org/articles/peutz-jeghers-syndrome-2
- ↑ "eMedicine - Peutz-Jeghers Syndrome : Article by Andrea Duchini, MD". Retrieved 2007-07-21.