Cytological features of bone marrow in multiple myeloma: atypical and binucleated plasma cells, Mott cells, clasmacytosis, and a phagocytosing macrophage.
Patient, 68 years old, diagnosed with multiple myeloma. Peripheral blood shows anemia, thrombocytopenia. Bone marrow is hypocellular, with binucleated plasma cells, signs of cytoplasmic clasmacytosis, Mott cells, and a macrophage in the first image..
🙏 The publication was kindly provided by KDL physician Alla Alekseenkova, CHUZ Clinical Hospital RZD-Meditsina, Smolensk.
A clinical case of multiple myeloma: 56% plasma cells in bone marrow aspirate, binucleated forms, and narrowed hematopoietic lineages.
A clinical case of multiple myeloma in a 65-year-old patient: bone marrow infiltration by atypical plasma cells up to 56%, cytoplasmic clasmatosis, and anemia.
Clinical case of bone marrow analysis after multiple myeloma treatment: erythroid lineage expansion to 47.5%, binucleated normoblasts, and mitoses.
