The aetiology of multiple myeloma is unknown (1).
The origin of the malignant clone in myeloma is the subject of debate but multistep genetic and microenvironmental changes appears to be responsible for the differentiation into malignant plasma cells (2).
The proliferating cells in myeloma occur principally in the bone marrow causing diffuse infiltration and localised solid tumours.
The myeloma cells secrete an osteoclast stimulating factor that leads to marked bone erosion.
The main sites for myeloma involvement are the proximal long bones, the pelvis, the thoracic cage, the vertebral column and the skull.
Risk factors thought to be responsible for multiple myeloma include:
Reference:
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