hemophagocytosis

he·mo·phag·o·cy·to·sis

(hē'mō-fag'ō-sī-tō'sis),
The process of engulfment (and usually destruction) of blood cells by the various types of phagocytic cells; used especially with reference to the engulfment of erythrocytes and others of the erythroid series.

hemophagocytosis

(hē″mō-făg″ō-sī-tō′sĭs) [″ + ″ + ″ + osis, condition]
The ingestion of red blood cells by phagocytes.
References in periodicals archive ?
Viruses produce thrombocytopenia by various mechanisms like impaired platelet production as a result of direct viral invasion, toxic effect of viral proteins on thrombopoiesis, virus-induced hemophagocytosis and increased platelet destruction by binding of virus-induced autoantibodies or viral antigen-antibody complexes.
However, bone marrow biopsy did not show hemophagocytosis or relapsing leukemia; therapy was started with biweekly etoposide and high-dose dexamethasone with some improvement of her fever.
The residual lymph node showed reactive germinal centers and tingible body macrophages, but no hemophagocytosis (Figure 1).
Peripheral blood smear and bone marrow aspiration were normal in terms of hemophagocytosis.
Microscopically, it is characterized by anastomosing and cyst-like vascular channels with papillary projections lined by sloughed plump endothelial cells often showing hemophagocytosis.
The diagnosis may be established genetically (based on mutations of the genes loci PRF1, UNC13D, or STX11) or by fulfillment of 5 out of 8 criteria: fever; splenomegaly; cytopenia; hypertriglyceridemia; hypofibrinogenemia; hemophagocytosis in the bone marrow, spleen, or lymph nodes; low or absent natural killer cell activity; and an elevated ferritin level (>500 ng/mL).
Hemophagocytic lymphohistiocytosis (HLH) is a condition characterized by fever, pancytopenia, hyperferritinemia, hypertriglyceridemia and hemophagocytosis in the bone marrow (5).
Histologic examination of bone marrow showed many activated macrophages, including some with hemophagocytosis (online Technical Appendix, http://wwwnc.
Indeed, occult HLH is often present and, although it was clinically and biologically ruled out in the case presented here, it is possible that bone marrow examination would have provided evidence of hemophagocytosis (maybe explaining anemia and increased lactate dehydrogenase).
Hemophagocytosis, plasmacytosis, caseous necrosis, and granulomas can be observed in bone marrow of patients with tuberculosis.
6%, hemophagocytosis in bone marrow in 83%, HLH was diagnosed in one patient with Chedik - Higashi syndrome, in one patient with malaria, in one patient with typhoid fever and in one case with systemic juvenile idiopathic arthritis (sJIA).