Castleman
disease
Overview
Castleman disease is a rare disorder that
involves an overgrowth of cells in your body's lymph nodes. The most common
form of the disorder affects a single lymph node, usually in the chest or
abdomen. This form is called unicentric Castleman disease.
Multicentric Castleman disease, or MCD,
affects multiple lymph nodes throughout the body. There are 3 types:
1.
HHV-8-associated MCD. This type is associated with human
herpes virus type 8, called HHV-8, and human immunodeficiency virus, or HIV.
2.
Idiopathic MCD. The cause of this type is unknown. This
is also called HHV-8-negative MCD.
3.
POEMS-associated MCD. This type is associated with another
condition called POEMS syndrome. POEMS syndrome is a rare blood disorder that
damages your nerves and affects other parts of your body.
Treatment and outlook vary, depending on the
type of Castleman disease you have. The type that affects only one lymph node,
unicentric Castleman disease, can usually be successfully treated with surgery.
Symptoms
Many people with unicentric Castleman disease
don't notice any signs or symptoms. The enlarged lymph node may be found during
a physical exam or an imaging test for some unrelated problem.
Some people with unicentric Castleman disease
might have signs and symptoms that are more commonly seen in multicentric
Castleman disease, which may include:
·
Fever.
·
Unintended weight
loss.
·
Fatigue.
·
Night sweats.
·
Enlarged liver or
spleen.
The enlarged lymph nodes associated with
multicentric Castleman disease are most commonly found in the neck, collarbone,
underarm and groin areas.
When to see a doctor
If you notice an enlarged lymph node on the
side of your neck or in your underarm, collarbone or groin area, talk to your
health care provider. Also call your care team if you have a persistent feeling
of fullness in your chest or abdomen, fever, fatigue, or unexplained weight
loss.
Causes
It's not clear what causes Castleman disease.
However, infection by a virus called human herpes virus 8, or HHV-8, is
associated with the HHV-8 version of multicentric Castleman disease.
Studies have found that HHV-8 is
present in nearly all HIV-positive people who have Castleman disease and
in fewer than of half of HIV-negative people with Castleman disease.
Risk factors
Castleman disease can affect people of any
age. But the average age of people diagnosed with unicentric Castleman disease
is 35. Most people with the multicentric form are in their 50s and 60s. The
multicentric form is also slightly more common in men than in women.
The risk of developing multicentric Castleman
disease is higher in people who are infected with HIV.
Complications
People with unicentric Castleman disease
usually do well once the affected lymph node is removed. Multicentric Castleman
disease may lead to life-threatening infections or organ failure. People who
also have HIV/AIDS generally have the worst outcomes.
Diagnosis
After reviewing your medical history and doing
a detailed physical exam, your health care provider may recommend:
·
Blood
and urine tests, to help rule out
other infections or diseases. These tests also can reveal anemia and
abnormalities in blood proteins that are sometimes typical of Castleman
disease.
·
Imaging
tests, to look for
enlarged lymph nodes, liver or spleen. A CT scan of your neck, chest,
abdomen and pelvis may be used. Positron emission tomography, also known as PET
scans, may be used to diagnose Castleman disease and to assess whether a
treatment is effective.
·
Lymph
node biopsy, to distinguish
Castleman disease from other types of lymphatic tissue disorders, such as
lymphoma. A tissue sample from an enlarged lymph node is removed and examined
in the laboratory.
Treatment
Treatment depends on the type of Castleman
disease you have.
Unicentric Castleman
disease
Unicentric Castleman disease can be cured by
surgically removing the diseased lymph node. If the lymph node is in your chest
or abdomen — which is often the case — major surgery may be needed.
If surgical removal isn't possible, medicine
may be used to shrink the lymph node. Radiation therapy also may be an
effective way to destroy the affected tissue.
You'll need follow-up exams, including
imaging, to check for relapse.
Multicentric Castleman
disease
Treatment for multicentric Castleman disease
generally involves medicines and other therapies to control cell overgrowth. Specific
treatment depends on the extent of your disease and on whether you
have HIV or HHV-8 infection or both.
Treatment options for multicentric Castleman
disease may include:
·
Immunotherapy. The use of drugs such as siltuximab
(Sylvant) or rituximab (Rituxan) can block the action of a protein that is made
in excess in people who have multicentric Castleman disease.
·
Chemotherapy. This type of medicine can slow the
overgrowth of lymphatic cells. Your provider may recommend adding chemotherapy
if the disease doesn't respond to immunotherapy or if you have organ failure.
·
Corticosteroids. Drugs such as prednisone can help
control inflammation.
·
Antiviral
drugs. These drugs can
block the activity of HHV-8 or HIV if you have one or both
of those viruses.
Preparing for your
appointment
You may be referred to a provider who is
trained in treating blood disorders called a hematologist.
What you can do
·
Write down the
symptoms you have been experiencing and for how long.
·
Write down key medical
information, including other health problems.
·
Make a list of all
medicines, vitamins and supplements that you're taking.
Questions to ask your doctor:
·
What's the most likely
cause of my signs and symptoms?
·
What kinds of tests do
I need? Do they require any special preparation?
·
What treatment do you
recommend? Do I need surgery?
In addition to the questions that you've
prepared to ask your health care provider, don't hesitate to ask other
questions during your appointment.
What to expect from
your doctor
Your health care team is likely to ask you a
number of questions. Being ready to answer them may leave time to go over
points you want to spend more time on. You may be asked:
·
Do you have any other
health conditions, such as HIV/AIDS or Kaposi's sarcoma?
·
When did you first
begin experiencing symptoms?
·
Have your symptoms
been continuous or occasional?
·
How severe are your
symptoms?
·
Does anything seem to
improve your symptoms?
·
What, if anything,
appears to worsen your symptoms?
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