What are the symptoms of plasma cell neoplasms?
Symptoms of plasma cell neoplasms can include bone pain, fatigue, frequent infections, and anemia. Some patients may also experience kidney dysfunction, hypercalcemia (high calcium levels), and weight loss. In advanced cases, there may be symptoms related to organ damage such as neuropathy or fractures.
How are plasma cell neoplasms diagnosed?
Plasma cell neoplasms are diagnosed through a combination of blood tests to detect abnormal antibodies, urine tests for Bence Jones proteins, bone marrow biopsy to examine plasma cell abnormalities, and imaging studies such as X-rays, MRI, or PET scans to identify bone lesions or organ involvement.
What are the treatment options for plasma cell neoplasms?
Treatment options for plasma cell neoplasms include chemotherapy, targeted therapy, immunomodulatory drugs, corticosteroids, and stem cell transplants. Radiation therapy and supportive care may also be used to alleviate symptoms. Treatment plans are tailored to the individual based on disease progression and patient health factors.
What causes plasma cell neoplasms?
Plasma cell neoplasms are caused by the abnormal proliferation of a single clone of plasma cells, which can result from genetic mutations and possibly environmental factors. The exact cause is not fully understood, but risk factors include age, gender, and certain pre-existing conditions like monoclonal gammopathy of undetermined significance (MGUS).
Are plasma cell neoplasms hereditary?
Plasma cell neoplasms, such as multiple myeloma, are generally not considered hereditary. While there may be some genetic predisposition, the direct hereditary risk is low, and most cases occur sporadically without a clear family history.