The proteins in these clients come from plasma cells of the bone marrow. Even though these patients are at risk for diseases of the blood or bone marrow, they do not have cancer from it. However, they may progress to myeloma or lymphoproliferative disorders. Hence, the clinician must follow the patient every year. The frequency of office visits will, of course, depend on the severity of it [1, 2].
In essence, these cases have to do with production of a monoclonal protein or M-protein. Should progression take place, the patient develops malignancy of the blood. In any event, MGUS is especially common in elderly men as well as Africans and African-Americans. Three to four percent of the population who are at least 50 years old have it. The risk of malignant transformation is less than one percent annually [1, 2].
Most diagnoses of MGUS happen in offices where internal medicine specialists perform the evaluations. One important concern is that a client without symptoms can change at any time and develop something abnormal. In other words, the patient can progress to an abnormal situation, and this requires a clinical evaluation prior to the next office visit [1, 2].
Nevertheless, the occurrence of MGUS otherwise does not require any treatment. The outpatient examinations will detect it should that take place. Of those who become ill, the individual can develop Waldenström macroglobulinemia, primary amyloidosis, non-Hodgkin lymphoma, and, of course, multiple myeloma. Other possibilities include plasma cell leukemia and solitary plasmacytoma [1, 2].
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