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Whipple's disease is a rare condition that prevents the small intestines from properly absorbing nutrients. This is called malabsorption.
Whipple's disease is caused by infection with a bacteria called Tropheryma whippelii. The disorder mainly affects middle-aged white men.
Whipple's disease is extremely rare. Risk factors are unknown.
Symptoms usually start slowly. Joint paint is the most common initial symptom. After that, often several years later, symptoms of gastrointestinal (GI) infection develop. Other symptoms may include:
The doctor or nurse will perform a physical exam. This may show:
Tests to diagnose Whipple's disease may include:
This disease may also change the results of the following tests:
People with Whipple's disease need to take long-term antibiotics to cure any infections of the brain and central nervous system. An antibiotic called ceftriaxone is given through a vein (IV). It is followed by another antibiotic (such as trimethoprim-sulfamethoxazole) taken by mouth for up to 1 year.
If symptoms come back during antibiotic use, the antibiotic treatment may be changed.
Your health care provider should closely follow your progress, because signs of the disease can return after you finish therapy. Those who have nutritional deficiencies from malabsorption will also need to take dietary supplements.
Without treatment, the condition is usually fatal. Treatment relieves symptoms and can cure the disease.
Call your health care provider if you have persistent joint pain, abdominal pain, or diarrhea.
If you are being treated for Whipple's disease, call your health care provider if:
Maiwald M, von Herbay A, Relman DA. Whipple’s disease. In: Feldman M, Friedman LS, Brandt LJ, eds. Sleisenger and Fordtran’s Gastrointestinal and Liver Disease. 9th ed. Philadelphia, PA: Saunders Elsevier; 2010:chap 106.
West SG. Systemic diseases in which arthritis is a feature. In:Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, PA: SaundersElsevier; 2011:chap 283.