How is Waldenstrom Macroglobulinemia diagnosed?

See how Waldenstrom Macroglobulinemia is diagnosed. Which specialists are essential to meet, what tests are needed and other useful information for the diagnosis of Waldenstrom Macroglobulinemia


Waldenstrom Macroglobulinemia (WM) is a rare type of cancer that affects the bone marrow and lymphatic system. It is characterized by the overproduction of abnormal white blood cells called lymphoplasmacytic cells, which produce an excess of a protein called monoclonal immunoglobulin M (IgM). Diagnosing WM involves a combination of clinical evaluation, laboratory tests, and imaging studies.



Clinical Evaluation


The first step in diagnosing WM is a thorough clinical evaluation by a healthcare professional. The doctor will review the patient's medical history, including any symptoms they may be experiencing. Common symptoms of WM include fatigue, weakness, weight loss, night sweats, enlarged lymph nodes, and bleeding problems.



Laboratory Tests


Several laboratory tests are used to diagnose WM:



1. Blood Tests


A complete blood count (CBC) is performed to evaluate the levels of different blood cells. In WM, there is often an increase in lymphocytes and plasma cells. The CBC may also reveal anemia and low platelet counts. Additionally, a blood test called serum protein electrophoresis (SPEP) is conducted to detect the presence of abnormal proteins, including monoclonal IgM.



2. Bone Marrow Biopsy


A bone marrow biopsy is a crucial test for diagnosing WM. It involves the removal of a small sample of bone marrow from the hipbone or another suitable site. The procedure is usually performed under local anesthesia. The sample is then examined under a microscope to assess the presence of lymphoplasmacytic cells and the amount of monoclonal IgM protein.



3. Immunoglobulin Levels


Immunoglobulin levels, including IgM, IgG, and IgA, are measured through blood tests. In WM, there is typically an elevated level of IgM.



4. Serum Viscosity Test


WM can cause the blood to become thicker due to the high levels of monoclonal IgM. A serum viscosity test is performed to measure the thickness of the blood. If the blood is too viscous, it can lead to various symptoms such as blurred vision, dizziness, and bleeding problems.



Imaging Studies


Imaging studies are often conducted to assess the extent of the disease and identify any complications:



1. X-rays


X-rays may be taken to examine the bones for any signs of damage or fractures caused by WM.



2. Computed Tomography (CT) Scan


A CT scan provides detailed cross-sectional images of the body. It can help identify enlarged lymph nodes, organs affected by WM, and any complications such as fluid accumulation around the lungs or abdomen.



3. Magnetic Resonance Imaging (MRI)


An MRI uses powerful magnets and radio waves to create detailed images of the body. It may be used to evaluate the brain, spinal cord, or other specific areas affected by WM.



4. Positron Emission Tomography (PET) Scan


A PET scan involves the injection of a small amount of radioactive material into the body. It can help detect areas of increased metabolic activity, which may indicate the presence of cancer cells.



Confirming the Diagnosis


Once the clinical evaluation, laboratory tests, and imaging studies are completed, a diagnosis of Waldenstrom Macroglobulinemia can be confirmed. It is important to consult with a hematologist or oncologist who specializes in blood cancers for an accurate diagnosis and appropriate treatment plan.



Disclaimer: The information provided above is for educational purposes only and should not be considered as medical advice. If you suspect you have Waldenstrom Macroglobulinemia or any other medical condition, please consult with a qualified healthcare professional for an accurate diagnosis and appropriate treatment.


by Diseasemaps

Bone marrow biopsy, blood tests, PET and CT scans

9/8/17 by Lynda 1300

Bone marrow sample..

9/8/17 by cindy 400

An oncologist is key in diagnosing WM. For me, I was diagnosed as IgM MGUS (Monoclonal Gamopathy of Unknown Significance) first. This meant that I was over producing IgM white blood cells. Over several years they watched those numbers and did several bone marrow biopsies. Once the IgM cells (adult cells) had infiltrated the bone marrow to a number grater than 10%, I had crossed over to WM. This also included other symptoms that I had: heavy night sweats, peripheral neuropathy, shortness of breath, headaches, extreme fatigue. The critical tests to watch initially is the blood-work tests. This will tell the initial story, and if needed then a bone marrow biopsy.

9/9/17 by Greg Martin 2450

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