If signs or symptoms suggest that a person may have Waldenstrom macroglobulinemia
(WM), more exams and tests will be done. The most important ones will look for the
abnormal protein in the blood and the abnormal cells in the bone marrow.
You may find it confusing that this document on WM also discusses ways to diagnose
non-Hodgkin lymphoma. But WM is a type of lymphoma. Like other lymphomas, it
invades the bone marrow, lymph nodes and other organs.
Signs and symptoms
Some of the signs and symptoms of people with WM are similar to those of people with
other types of non-Hod gkin lymphomas (NHL) . For ex ample, weight loss, fever, night
sweats, and swollen lymph nodes can be seen in many types of NHL.
Other WM symptoms are caused by the abnormal antibody produced b y the cancer cells.
In hyperviscosity syndrome , too much of this protein can cause the blood to become too
"thick." (This is not the kind of thickness that can be treated with drugs known as "blood
thinners.") When the blood gets too thick, it has trouble traveling throu gh b lood vessels.
This causes poor circulation to the brain which can lead to problems similar to a stroke.
If the abnormal protein only causes the blood to become thick at cooler temperatures (like
in the hands and feet), it is called a cryoglobulin . Cryoglobulins can cause the hands and
feet to become painful in cool temperatures.
A condition called amyloidosis occurs when a p art of the abnormal antibody (called the
light chain) builds up in organs like the heart and kidneys. The protein buildup can
interfere with the function of these organs, leading to heart and kidney problems.
Not all patients with WM develop hyperviscosity, cryoglobulins or amyloidosis.
The most common symptoms of WM are:
Weakness :The most common symptom of WM is weakness. It can be caused b y anemia (low red
blood cells) which can happen when the lymphoma cells crowd out normal cells in the
bone marrow. Some people also feel weak when the blood becomes thick from the
abnormal protein.
Loss of appetite
About one-fourth of p atients lose their appetite.
Fever
Lymphoma can cause fevers (without an infection), drenchin g night sweats, and weight
loss. Together, these 3 symptoms are called B-symptoms .
Neuropathy
The abnormal antibody in some people with WM can attack and damage nerves outside
the brain. This can lead to problems with numbness or a painful "pins and needles"
sensation in the feet and legs, which is called Neuropathy
Other problems include:
Enlarged lymph nodes
These will usually appear as bumps under the skin around the neck, in the groin, or in the
armpits. Enlarged lymph nodes are usually about 1 or 2 inches in size in WM, but can be
bigger in other lymphomas.
Swollen abdomen
Lymphoma can cause the spleen or liver to enlarge, making the belly look swollen. In the
upper part of the abdomen, the liver is on the right and the spleen on the lef t. When the
spleen gets larger, it can press on the stomach — which makes people feel full when they
eat only a small amount.
Nervous system symptoms
In hyperviscosity syndrome, the thickened blood causes poor brain circulation leading to
problems like headache, confusion, and dizziness. It can also cause symptoms like those
seen with a stroke, including slurred speech and weakness on one side of the body.
Patients with these symptoms should contact their doctor right away.
Abnormal bleeding
High levels of abnormal antibody protein can damage blood vessels. Nosebleeds and bleeding gums are common symptoms of people with WM.
Vision problems
Bleeding around the small blood vessels inside the eyes might cause blurred vision or
blind spots. If the blood becomes thick from the abnormal antibody protein, it leads to
slow circulation through the blood vessels in the eye, which can also interfere with
vision.
Kidney problems
WM can damage the kidneys in 2 ways. First of all, the abnormal antibody protein can
damage the kidneys directly. Secondly, if amyloidosis develops, the abnormal protein
builds up in the kidneys, so they don't work well. When the kidneys aren't working well,
excess salt, fluid, and body waste products stay in the blood. The resulting symptoms
include weakn ess, trouble breathin g, and fluid buildup in body tissues.
Heart problems
There are several causes of heart problems in WM. High levels of abnormal antibody
protein can directly damage h eart tissue. Also, in amyloidosis, this abnormal protein
builds up in the heart muscle. This makes the heart weaker and impairs its ability to pump
blood properly. In addition, because the blood of people with WM is "thicker" than
normal, their hearts have to work harder to pump blood throughout the body. This strain
can cause the heart to "wear out," a condition called congestive heart failure . Symptoms
of congestive heart failure include weakness, shortness of breath, and swelling in the f eet
and legs.
Infections
The high levels of abnormal antibody in WM "turn-off" normal antibody production.
This makes it harder for the body to resist infections.
Laboratory tests
The diagnosis of WM may be suspected if your doctor finds low blood counts or unusual
protein levels on blood tests. This is followed by a test to characterize the proteins called
serum electrophoresis . It is usually only after these tests are done that a biopsy of either
the bone marro w or a lymph node is considered.
Blood counts The complete blood count (CBC) is a test that measures the levels of red cells, white
cells, and platelets in the blood. If the lymphoma cells occupy too much of the bone marrow, these levels will be low.
Quantitative immunoglobulins
This test measures the blood levels of the different antibodies. There are several different types of antibodies in the blood: IgA, IgE, IgG, and IgM. The levels of these
immunoglobulins are measured to see if any are abnormally high or low. In WM the level
of IgM is high but the IgG level is often low.
Electrophoresis
The immunoglobulin produced in WM is IgM. It is abnormal because it is monoclonal —
meaning that it is just many copies of the ex act same antibody. Serum protein
electrophoresis (or SPEP) is a test that measures the total amount of immunoglobulins in
the blood and finds any abnormal (monoclonal) immunoglobulin. Then, another test, such
as immunofixation or immunoelectrophoresis, is used to determine the type of antibody
that is abnormal (IgM or some other type).
Finding a monoclonal IgM immunoglobulin in the blood is necessary to make a diagnosis
of WM. The abnormal protein in WM is known by several differ ent names, including
monoclonal immunoglobulin M , IgM protein , IgM spike , IgM paraprotein , and M-spike .
Other typ es of monoclonal immunoglobulins, like IgA or IgG, are seen in different
disorders (like multiple myeloma and some lymphomas).
Sometimes pieces of the IgM protein are excreted by the kidneys into the urine. The
procedure used for finding that protein is called urine protein electrophoresis (or UPEP).
Viscosity
Viscosity measures how thick the blood is. If the IgM level is too high, it will cause the
blood to become thick (viscous) so that it can't flow freely. Think about pouring honey
compared to pouring water. If the blood becomes too thick, the brain doesn't get enough
blood and oxygen. This can be treated with plasmapheresis.
Cryocrit
This tests the blood for a cryoglobulin (a protein that causes the blood to clump together
in cool temperatures).
Beta-2-microglobulin
This is another protein produced by the cancer cells in WM. This protein itself doesn't
cause any problems, but it is a useful indicator of a patient’s pro gnosis (outlook). High
levels mean a poor outlook.
Types of biopsies
The symptoms of WM and NHL are not unique enough for a doctor to know for certain if
cancer is present. Most symptoms can also be caused by non-can cerous problems like
infections or by other kinds of cancers. A biopsy is the only way to make an accurate
diagnosis. There are several biopsy procedu res. Doctors choose which to use based on the
unique aspects of each patient's situation.
Bone marrow aspiration and biopsy
This test is necessary to diagnose WM. It can be done at the doctor's office or at the
hospital. First, an area at the back of the hip/pelvis bone is numbed with a local
anesthetic. Then, to do the bone marrow aspiration, a needle is inserted into the bone, and
a syringe is used to remove some bone marrow. Even with the numbing medicine, this
often causes a brief, sharp pain.
For the bone marrow biopsy, a needle is used to remove a cylinder of bone and marrow,
about 1/16-inch across and 1-inch long. With the numbing medicine, most patients feel
pressure for this part, but not pain.
There is some soreness in the biopsy area when the numbing medicine wears off. Most
patients can go home immediately after the procedure. The bone marrow is then
examined under the microscope (by a doctor called a pathologist ) to see if lymphoma
cells are p resent. In WM, at least 10% of the cells in the bone marrow are
lymphoplasmacytoid lymphoma.
Fine needle aspiration biopsy
Fine needle aspiration (FNA) biopsy uses a very thin needle with a syringe to withdraw a
small amount of tissue from a tumor or lymph node. The doctor can aim the needle while
feeling an enlarged node near the surface of the body. If the tumor is deep inside the
body, the needle can be guided while it is viewed by a computed tomography (CT) scan
(see the descriptions of imaging tests later in this section).
The main advantage of FNA is that the patient will not require surgery for this procedure.
The disadvantage is that in some cases the thin needle cannot remov e enough tissue for a
definite diagnosis of lymphoma. However, adv ances in performin g flow cytometry and
molecular genetic studies (discussed later in this section) and the growing experience of
many doctors with FNA have improved the accu racy of this procedure.
FNA is very useful in diagnosing cancers that have spread to nodes from other organs
and in identifying nodes swollen by infection that don’t need to be removed. FNA is
useful in diagnosing some lymphomas, but it is less helpful for WM because the
diagnosis is usually made with a bone marrow biopsy.
Fat pad aspiration
In this procedure, a needle with a syringe attached is inserted into an area of fat (usually
the skin of the abdomen/belly). Then, a small amount of fat is removed and sent to the lab
for testing. This may be used in WM to check for amyloid.
Excisional or incisional biopsy
For these types of biopsies, a surgeon cuts through the skin to remove an entire lymph
node or tumor (excisional biopsy) or a just a small part of a large tumor or lymph node
(incisional biopsy). If the area to b e biopsied is near the skin surface, this can be done
using just a local anesthesia (numbing medicine). If the area is inside the chest or
abdomen, general an esthesia or deep sedation is used (the patient is asleep). The
excisional and incisional methods almost always provide enough tissue to diagnose the
exact type of lymphoma. These biopsies ar e rarely needed in people with WM because
the diagnosis is usually made with a bone marrow biopsy. They are used more often for
other types of lymphoma.
Laboratory tests on biopsy specimens
All biopsy specimens are examined under a microscope b y a pathologist – a doctor with
special training in recognizing cells from blood and lymphoid tissue diseases. The doctor
looks at the size and shape of the cells and how the cells are arranged in the lymph node
or bone marrow. Sometimes this exam does not provide a definite answer and other
laboratory tests are needed.
Immunohistochemistry
In this test, a part of the biopsy sample is treated with special laboratory antibodies so
that certain types of cells change color. The color change can be seen under a
microscope. This test may be helpful in distinguishing different types of lymphoma from
one another and from other diseases.
Flow cytometry
In this test, cells are treated with special laboratory antibodies and passed in front of a
laser beam. Each antibody sticks only to certain types of cells. If the sample contains
those cells, the laser light will cause them to give off light of a different color, which is
measured exactly and analyzed by a computer. Th is test can help determine whether
lymph node swelling is because of lymphoma, some other can cer, or a non -cancerous
disease. It has become increasin gly important in helping doctors determine the exact type
of lymphoma so they can select the best treatment.
Cytogenetics
For this technique, cells (usually from the bone marrow) are cultured in the lab to get
them to divide so that the chromosomes can be seen. Then the chromosomes are stained
and a microscop e is used to examine them. Because it takes time for the cells to start
dividing, this test can take weeks.
Normal human cells each contain 46 chromosomes (pieces of DNA that co ntrol the cells’
growth and metabolism). In some lymphomas, part of one chromosome is attached to part
of a different chromosome, this is called a translocation . In WM it is more common for
the lymphoma cells to be missing part of a chromosome (called a deletion ) .
Molecular genetic studies
These tests are not usually necessary to diagnose WM, but are sometimes used to
diagnose other types of NHL. These tests look at the cells’ DNA without having to gro w
the cells in the lab first, and can be done on cells from different sources (like lymph
nodes, blood, and bone marrow)._Th ey are generally used to look for certain genetic
changes, not just any change.
One test that can be done is to look at the DNA that contains information on each cell's
antigen receptors. Normal lymphoid tissue contains cells with many different antigen
receptors, helping the body respond to many types of infection. Because lymphoma starts
from a single abnormal cell, all cells in each patient have the same antigen receptor. This
is a complex test and may not be needed in every case.
Tests of lymphoma cell DNA can also find chromosome changes that are characteristic of
certain types of NHL. This can be helpful in determining what kind of lymphoma is
present.
Usually genetic tests aren't needed to diagnose WM, but they may be very useful for
research.
Imaging tests
Imaging tests may be done to look for an enlarged spleen and lymph nod es. Finding these
is not needed to diagnose WM.
Chest x-ray
Plain x-rays may detect enlarged lymph nodes in the chest.
Computed tomography
The computed tomography (CT) scan is an x-ray procedure that produces detailed cross-
sectional images of your body. Instead of taking one picture, like a conventional x-ray, a
CT scanner tak es many pictures as it rotates around you. A computer then combines these
pictures into an image of a slice of your bod y. The machine creates multiple images of
the part of your body that is being studied. A CT scan is useful for looking at lymphoma
in the abdomen, pelvis, and chest.
You may be asked to drink 1 to 2 pints of a solution of contrast material before the scan.
This helps outline the intestine so that it is not mistaken for tumors. You may also receive
an intravenous (IV, in the vein) line through which a different contrast dye is injected.
This helps better outline structures in your body. The injection can cause a feeling of
warmth throughout the body (flushing). Some people are allergic to the IV contrast and
get hives. Rarely, more serious reactions like trouble breathing and low blood pressure
can occur. Medication can be given to prevent and treat allergic reactions. Be sure to tell
the doctor if you have ever had a reaction to any contrast material used for x-rays.
CT scans can tak e longer than regular x-rays. You must lie still on a table while they are
being done. But many just take a few minutes. You might feel a bit confined by the
machine you lie in when the pictures are being tak en.
CT scans can also be used to precisely guide a bio psy needle into an enlarged lymph
node. For this procedure, called a CT-guided needle biopsy , the patient remains on the CT
scanning table while a radiologist moves a biopsy needle toward the mass. CT scans are
repeated until the doctors are sure that the needle is within the mass. A fine needle biopsy
(tiny fragment of tissue) or a core needle biopsy (a thin cylinder of tissue about ½-inch
long and less than 1/8-inch in diameter) sample is removed and examined under a
microscope.
Magnetic resonance imaging
Magnetic resonance imagin g (MRI) scans use rad io waves and strong magnets instead of
x-rays. The energy from the radio waves is absorbed and then released in a pattern
formed by the type of tissue and by certain diseases. A computer translates the pattern of
radio waves given off by the tissues into a very detailed image of parts of the body. Not
only does this produce cross-sectional slices of the body like a CT scanner, it can also
produce slices that are parallel with the length of your body. Sometimes a contrast
material is injected into a vein to make some structures clearer. This contrast is not the
same as the contrast used for CT scans, but allergic reactions can still occur . Again,
medicine can b e given to prevent and treat allergic reactions.
MRI scans are helpful in examining the brain and spinal cord. MRI scans are a little more
uncomfortable than CT scans. First, they take longer -- about an hour. Also, you have to
lie inside a tube, which is confining and can upset people with a fear of enclosed spaces.
The machine also makes a thumping noise that some people find disturbing. Some places
provide headphones with music to block this noise out. If you have problems with close
spaces (claustrophobia), you should let your docto r know befo re the MRI scan.
Positron emission tomography
A positron emission tomography (PET) scan uses a form of sugar (glucose) that has a
radioactive atom. A special camer a can detect the radioactivity. Cancer cells absorb
higher amounts of the radioactive sugar than normal tissue does because of their high rate
of metabolism. PET is useful to look for lymphoma throughout your body. It is
sometimes used to tell if an enlarged lymph node contains lymphoma or is benign. This
can be helpful after treatment to see if an enlar ged lymph node still contains lymphoma
or is merely scar tissue.
