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Peutz-Jeghers syndromeDefinition Peutz-Jeghers syndrome (PJS) is a disorder characterized by intestinal polyps. In addition, pigmented spots develop from infancy through childhood around the lips, gums, mucous membranes, and skin. The polyps develop most commonly in the small intestine, but also in the colon. There may be a significant risk of these polyps becoming malignant and thus of patients developing cancer. Some studies link PJS and cancers of the gastrointestinal tract, lung, breast, uterus, and ovaries. There are two types of PJS -- "familial" PJS, which is inherited, and "sporadic" PJS, which is not. Causes, incidence, and risk factors When inherited, Peutz-Jeghers syndrome is transmitted as an autosomal dominant trait. This means that, on average, each child of someone with familial PJS has a 50-50 chance of inheriting PJS. Symptoms
Signs and tests
Tests
Treatment Surgery may be needed to remove polyps that cause chronic problems. Iron supplements help counteract blood loss. In addition, the patient should be monitored periodically to watch for malignant changes in polyps. Comprehensive surveillance guidelines can be found at geneclinics.org. A booklet with additional information by Johns Hopkins University is available at hopkins-coloncancer.org. Support Groups An electronic mailing list (discussion group) is available at acor.org. Expectations (prognosis) The outcome varies depending on what problems develop. Complications
Calling your health care provider Call for an appointment with your health care provider if symptoms of this condition are present. Severe abdominal pain indicates a possible emergency condition such as intussusception. If you are planning to have children and there is a family history of this condition, it may be helpful to talk with your health care provider. Prevention Genetic counseling is recommended for prospective parents with a family history of Peutz-Jeghers syndrome. Genetic counselors can be located through the Cancer Genetics Services Directory. Illustrations
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