Peutz-Jeghers syndrome (patient information): Difference between revisions

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==When to seek urgent medical care?==
==When to seek urgent medical care?==
==Diagnosis==
==Diagnosis==
*The polyps develop mainly in the small intestine, but also in the large intestine (colon). An exam of the colon called a colonoscopy will show colon polyps. The small intestine is evaluated in 2 ways. One is a barium x-ray (small bowel series).
*The other is a capsule endoscopy, in which a small camera is swallowed and then takes many pictures as it travels through the small intestine.
Additional exams may show:
*Part of the intestine folded in on itself (intussusception)
*Benign (noncancerous) tumors in the ear
Laboratory tests may include:
*Complete blood count -- may reveal anemia
*Genetic testing
*Stool guaiac, to look for blood in stool
*Total iron-binding capacity (TIBC) -- may be linked with iron-deficiency anemia


==Treatment options==
==Treatment options==

Revision as of 15:47, 19 December 2017


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Peutz-Jeghers syndrome

Overview

What are the symptoms?

What are the causes?

Who is at highest risk?

When to seek urgent medical care?

Diagnosis

Treatment options

Prevention

Where to find medical care for Peutz-Jeghers syndrome?

What to expect (Outlook/Prognosis)?

Possible complications

Prevention

Peutz-Jeghers syndrome On the Web

Ongoing Trials at Clinical Trials.gov

Images of Peutz-Jeghers syndrome

Videos on Peutz-Jeghers syndrome

FDA on Peutz-Jeghers syndrome

CDC on Peutz-Jeghers syndrome

Peutz-Jeghers syndrome in the news

Blogs on Peutz-Jeghers syndrome

Directions to Hospitals Treating Peutz-Jeghers syndrome

Risk calculators and risk factors for Peutz-Jeghers syndrome

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Peutz-Jeghers syndrome (PJS) is a disorder in which growths called polyps form in the intestines. It is passed down through families (inherited). A person with PJS has a high risk of developing certain cancers.

What are the symptoms of Peutz-Jeghers syndrome?

Symptoms of PJS are:

  • Brownish or bluish-gray spots on the lips, gums, inner lining of the mouth, and skin
  • Clubbed fingers or toes
  • Cramping pain in the belly area
  • Dark freckles on and around the lips of a newborn
  • Blood in the stool that can be seen with the naked eye (sometimes)
  • Vomiting

What causes Peutz-Jeghers syndrome?

  • It is unknown how many people are affected by PJS. However, the National Institutes of Health estimates that it affects about 1 in 25,000 to 300,000 births.
  • There are 2 types of PJS:
    • Familial PJS may be due to a mutation in a gene called STK11. The genetic defect can be inherited through families as an autosomal dominant trait. That means if 1 of your parents has this type of PJS, you have a 50% chance of inheriting the gene and having the disease.
    • Sporadic PJS is not passed down through families and appears unrelated to an STK11 gene mutation.

Who is at highest risk?

When to seek urgent medical care?

Diagnosis

  • The polyps develop mainly in the small intestine, but also in the large intestine (colon). An exam of the colon called a colonoscopy will show colon polyps. The small intestine is evaluated in 2 ways. One is a barium x-ray (small bowel series).
  • The other is a capsule endoscopy, in which a small camera is swallowed and then takes many pictures as it travels through the small intestine.

Additional exams may show:

  • Part of the intestine folded in on itself (intussusception)
  • Benign (noncancerous) tumors in the ear

Laboratory tests may include:

  • Complete blood count -- may reveal anemia
  • Genetic testing
  • Stool guaiac, to look for blood in stool
  • Total iron-binding capacity (TIBC) -- may be linked with iron-deficiency anemia

Treatment options

Where to find medical care for Peutz-Jeghers syndrome?

Directions to Hospitals Treating Peutz-Jeghers syndrome

What to expect (Outlook/Prognosis)?

Possible complications

Sources