Whipple's
disease
Overview
Whipple disease is a rare bacterial infection
that most often affects your joints and digestive system. Whipple disease
interferes with normal digestion by impairing the breakdown of foods, and
hampering your body's ability to absorb nutrients, such as fats and
carbohydrates.
Whipple disease can also infect other organs,
including your brain, heart and eyes.
Without proper treatment, Whipple disease can
be serious or fatal. However, a course of antibiotics can treat Whipple
disease.
Symptoms
Common signs and
symptoms
Digestive signs and symptoms are common in
Whipple disease and may include:
·
Diarrhea
·
Stomach cramping and
pain, which may worsen after meals
·
Weight loss,
associated with the malabsorption of nutrients
Other frequent signs and symptoms associated
with Whipple disease include:
·
Inflamed joints,
particularly the ankles, knees and wrists
·
Fatigue
·
Weakness
·
Anemia
Less common signs and
symptoms
In some cases, signs and symptoms of Whipple
disease may include:
·
Fever
·
Cough
·
Enlarged lymph nodes
·
Skin darkening in
areas exposed to the sun and in scars
·
Chest pain
Brain and nervous system (neurological) signs
and symptoms may include:
·
Difficulty walking
·
Vision problems,
including lack of control of eye movements
·
Confusion
·
Memory loss
Symptoms tend to develop slowly over many
years in most people with this disease. In some people, symptoms such as joint
pain and weight loss develop years before the digestive symptoms that lead to
diagnosis.
When to see a doctor
Whipple disease is potentially
life-threatening yet usually treatable. Contact your doctor if you experience
unusual signs or symptoms, such as unexplained weight loss or joint pain. Your
doctor can perform tests to determine the cause of your symptoms.
Even after the infection is diagnosed and
you're receiving treatment, let your doctor know if your symptoms don't
improve. Sometimes antibiotic therapy isn't effective because the bacteria are
resistant to the particular drug you're taking. The disease can recur, so it's
important to watch for symptoms that reappear.
Causes
Whipple disease is caused by a type of
bacterium called Tropheryma whipplei. The bacteria affect the mucosal lining of
your small intestine first, forming small sores (lesions) within the wall of
the intestine. The bacteria also damage the fine, hairlike projections (villi)
that line the small intestine.
Not much is known about the bacteria. Although
they seem readily present in the environment, scientists don't know where they
come from or how they're spread to humans. Not everyone who carries the
bacteria develops the disease. Some researchers believe that people with the
disease may have a genetic defect in their immune system response that makes
them more likely to become sick when exposed to the bacteria.
Whipple disease is extremely uncommon,
affecting fewer than 1 in 1 million people.
Risk factors
Because so little is known about the bacteria
that cause Whipple disease, risk factors for the disease haven't been clearly
identified. Based on available reports, it appears more likely to affect:
·
Men ages 40 to 60
·
White people in North
America and Europe
·
Farmers and other
people who work outdoors and have frequent contact with sewage and wastewater
Complications
The lining of your small intestine has fine,
hairlike projections (villi) that help your body absorb nutrients. Whipple
disease damages the villi, impairing nutrient absorption. Nutritional
deficiencies are common in people with Whipple disease and can lead to fatigue,
weakness, weight loss and joint pain.
Whipple disease is a progressive and
potentially fatal disease. Although the infection is rare, associated deaths
continue to be reported. This is due in large part to late diagnoses and
delayed treatment. Death often is caused by the spread of the infection to the
central nervous system, which can cause irreversible damage.
Diagnosis
The process of diagnosing Whipple disease
typically includes the following tests:
·
Physical
exam. Your doctor
generally begins with a physical exam. He or she will look for signs and
symptoms that suggest the presence of this condition. For example, your doctor
may look for stomach tenderness and skin darkening, particularly on sun-exposed
parts of your body.
·
Biopsy. An important step in diagnosing Whipple
disease is taking a tissue sample (biopsy), usually from the lining of the
small intestine. To do this, your doctor typically performs an upper endoscopy.
The procedure uses a thin, flexible tube (scope) with a light and a camera
attached that passes through your mouth, throat, windpipe and stomach to your
small intestine. The scope allows your doctor to view your digestive passages
and take tissue samples.
During the procedure, doctors remove tissue samples from several
sites in the small intestine. A doctor examines this tissue under a microscope
in a lab. He or she looks for the presence of disease-causing bacteria and
their sores (lesions), and specifically for Tropheryma whipplei bacteria. If
these tissue samples don't confirm the diagnosis, your doctor might take a
tissue sample from an enlarged lymph node or perform other tests.
In some cases, your doctor may ask you to swallow a capsule that
holds a small camera. The camera can take images of your digestive passages for
your doctor to view.
A DNA-based test known as polymerase chain reaction, which is
available at some medical centers, can detect Tropheryma whipplei bacteria in
biopsy specimens or spinal fluid samples.
·
Blood
tests. Your doctor may
also order blood tests, such as a complete blood count. Blood tests can detect
certain conditions associated with Whipple disease, particularly anemia, which
is a decline in the number of red blood cells, and low concentrations of
albumin, a protein in your blood.
Treatment
Treatment of Whipple disease is with antibiotics,
either alone or in combination, which can destroy the bacteria causing the
infection.
Treatment is long-term, generally lasting a
year or two, with the aim of destroying the bacteria. But symptom relief
generally comes much quicker, often within the first week or two. Most people
with no brain or nervous system complications recover completely after a full
course of antibiotics.
When choosing antibiotics, doctors often
select those that wipe out infections in the small intestine and also cross a layer
of tissue around your brain (the blood-brain barrier). This is done to
eliminate bacteria that may have entered your brain and central nervous system.
Because of the lengthy use of antibiotics,
your doctor will need to monitor your condition for development of resistance
to the drugs. If you relapse during treatment, your doctor may change your
antibiotics.
Treatment for standard
cases
In most cases, Whipple disease therapy begins
with two to four weeks of ceftriaxone or penicillin given through a vein in
your arm. Following that initial therapy, you'll likely take an oral course of
sulfamethoxazole-trimethoprim (Bactrim, Septra) for one to two years.
Possible side effects of ceftriaxone and
sulfamethoxazole-trimethoprim include allergic reactions, mild diarrhea, or
nausea and vomiting.
Other medications that have been suggested as
an alternative in some cases include oral doxycycline (Vibramycin, Doryx,
others) combined with the antimalarial drug hydroxychloroquine (Plaquenil),
which you'll likely need to take for one to two years.
Possible side effects of doxycycline include
loss of appetite, nausea, vomiting and sensitivity to sunlight.
Hydroxychloroquine may cause loss of appetite, diarrhea, headache, stomach
cramps and dizziness.
Symptom relief
Your symptoms should improve within one to two
weeks of starting antibiotic treatment and go away entirely within about one
month.
But even though symptoms improve quickly,
further lab tests may reveal the presence of the bacteria for two or more years
after you begin taking antibiotics. Follow-up testing will help your doctor
determine when you can stop taking antibiotics. Regular monitoring can also
detect development of resistance to a particular drug, often indicated by a
lack of improvement in symptoms.
Even after successful treatment, Whipple
disease can recur. Doctors usually advise regular checkups. If you've
experienced a recurrence, you'll need to repeat antibiotic therapy.
Taking supplements
Because of the nutrient-absorption
difficulties associated with Whipple disease, your doctor may recommend taking
vitamin and mineral supplements to ensure adequate nutrition. Your body may
require additional vitamin D, folic acid, calcium, iron and magnesium.
Preparing for your
appointment
If you have signs and symptoms common to
Whipple disease, make an appointment with your doctor. Whipple disease is rare,
and the signs and symptoms can indicate other, more common disorders, so it can
be hard to diagnose. As a result, it's often diagnosed in its later stages. However,
an early diagnosis reduces the risk of serious health effects associated with
not treating the condition.
If your doctor is uncertain about the
diagnosis, he or she may refer you to a doctor who specializes in digestive
diseases or to another specialist depending on the symptoms you're having.
Here's some information to help you get ready
for your appointment, and know what to expect from your doctor.
Information to gather
in advance
·
Write
down your symptoms, including when
you first noticed them and how they may have changed or worsened over time.
·
Write
down your key medical information, including other conditions with which you've been
diagnosed and the names of all medications, vitamins and supplements you're
taking.
·
Write
down key personal information, including any recent changes or stressors in your life.
These factors can be connected to digestive signs and symptoms.
·
Take
a family member or friend along, if possible. Someone who accompanies you may remember
something that you missed or forgot.
·
Write
down questions to ask your doctor.
Creating your list of questions in advance can help you make the most of your
time with your doctor.
For signs and symptoms common to Whipple
disease, some basic questions to ask your doctor include:
·
What is the most likely
cause of my condition?
·
Are there any other
possible causes for my condition?
·
What diagnostic tests
do I need?
·
What treatment
approach do you recommend?
·
I have other medical
conditions. How do I manage them together?
·
How soon do you expect
my symptoms to improve with treatment?
·
For how long will I
need to take medications?
·
Am I at risk of
complications from this condition?
·
Am I at risk of a
recurrence?
·
How often will you
need to see me for monitoring?
·
Do I need to change my
diet?
·
Should I take any nutritional
supplements?
·
Are there any
lifestyle changes I can make to help reduce or manage my symptoms?
Don't hesitate to ask any other questions you
have.
What to expect from
your doctor
A doctor who sees you for possible Whipple
disease is likely to ask a number of questions, such as:
·
What are your
symptoms, and when did you notice them?
·
Have your symptoms
gotten worse over time?
·
Are your symptoms
typically worse after a meal?
·
Have you lost weight
without trying?
·
Do your joints hurt?
·
Do you feel weak or fatigued?
·
Do you have difficulty
breathing or a cough?
·
Have you developed
confusion or memory problems?
·
Have you noticed
problems with your eyes or vision?
·
Has anyone close to
you had similar signs or symptoms recently?
·
Have you been
diagnosed with any other medical conditions, including food allergies?
·
Do you have any family
history of bowel disorders or colon cancer?
·
What medications do
you take, including prescription and over-the-counter medications, vitamins,
herbs, and supplements?
·
Are you allergic to
any medications?
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