Hi,I am Dr. Shanthi.E (General & Family Physician). I will be looking into your question and guiding you through the process. Please write your question below.
Hi,I am Dr. Shanthi.E (General & Family Physician). I will be looking into your query and guiding you through the process. Please write your question below.
Whipple's disease is a rare condition that prevents the intestine from properly absorbing nutrients. This is called malabsorption.
Causes :
Whipple's disease is caused by infection from bacteria called Tropheryma whippelii.
The disorder mainly affects middle-aged white men.
Whipple's disease is extremely rare. Risk factors are unknown.
Symptoms :
Symptoms usually start slowly, and may include:
Abdominal pain
Diarrhea
Fever
Gray to brown skin color
Joint pain
Memory loss
Mental changes
Weight loss
Exams and Tests :
Possible signs:
Enlarged lymph glands
Fatty stools
Gastrointestinal bleeding
Swelling in body tissues (edema)
Tests may include:
Viewing the intestine with a flexible, lighted tube (enteroscopy), and possibly removing a small amount of intestinal lining (biopsy) to be examined under the microscope
This disease may also change the results of the following tests:
Albumin
Unabsorbed fat in the stools (fecal fat)
Intestinal absorption of a type of sugar (d-xylose absorption)
Treatment :
You will need to take long-term antibiotics to cure any infections of the brain and central nervous system. A medicine called ceftriaxone is given through a vein (IV). It is followed by an 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 you, 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.
Prognosis :
Without treatment, the condition is usually fatal. Treatment relieves symptoms and can cure the disease.
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