Other names that are sometimes used for WM include: lymphoplasmacytic lymphoma, lymphoplasmacytic leukemia,
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Waldenstrom's macroglobulinemia is not considered hereditary, as most cases occur sporadically without a clear genetic link. However, some studies suggest a potential association with certain genetic predispositions, particularly in families with other lymphoproliferative disorders. While having a family history of related conditions may slightly increase risk, the majority of patients do not have a direct hereditary connection. Always consult a healthcare professional for personalized information regarding risk factors.
Many individuals with WM have no symptoms of the disease. This is known as asymptomatic macroglobulinemia. When symptoms of WM are present, they may vary greatly
There is no known prevention for WM
All lymphomas other than Hodgkin's disease, including WM, are known collectively as non-Hodgkin's lymphomas.
It was first identified in 1944, by the Swedish physician Jan Gosta Waldenstrom
Since many individuals with WM have no symptoms, the initial diagnosis may result from blood tests that are performed for some other purpose.
There also is no generally-accepted course of treatment for WM.
It is estimated that it may affect about five out of every 100,000 people
WM most often affects males over the age of 65
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Biological therapy or immunotherapy, with the potent, immune system protein interferon alpha, is used to relieve the symptoms of WM.