ABSTRACT
Multiple myeloma is a condition of malignant plasma cell proliferation derived from a single B-cell lineage. These cells produce monoclonal immunoglobulins, most commonly either immunoglobulin G (IgG) or immunoglobulin A (IgA). The peak incidence of MM is in the seventh decade, whereas, it is a rare entity in young patients. Here we are presenting a case report of 33 years old male patient with diagnosis of Multiple myeloma WHERE are able to find and document the classical features of Multiple myeloma. Increased level of β2 microglobulin, serum creatinine, IL-6, IL-2 and plasmablastic type myeloma cells suggest poor prognosis of mm patients.
ABSTRACT
Neuroblastoma is one of the most common childhood malignancies. Patients diagnosed under 1 years of age (40%) have a much better prognosis than those diagnosed in later childhood. Neuroblastoma originates from neural crest cells of the adrenal medulla or sympathetic ganglia. Neuroblastomas commonly present as an asymptomatic mass in a child. The treatment of neuroblastoma depends on the stage, and it includes surgical excision, multi agent chemotherapy, and bone marrow transplantation.