2019
DOI: 10.1136/postgradmedj-2019-136512
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Secondary haemophagocytic lymphohistiocytosis associated with metronidazole

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Cited by 3 publications
(3 citation statements)
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“…Clinical patterns range between signs and symptoms of sepsis, SIRS, shock and multi-organ failure [2]. Diagnosis is confirmed when at least 5 out of 8 criteria are met [3]: (1) fever; (2) Splenomegaly; (3) Cytopenias affecting 2 of 3 lineages in the peripheral blood: a) hemoglobin less than 90 g/L or less than 100 g/L in infants < 4 weeks; b) Platelets less than 100 x10 9 /L; c) Neutrophils less than 1.0 x 10 9 /L; (4) Hypertriglyceridemia and/or hypofibrinogenemia; (5) Hemophagocytosis in bone marrow, spleen or lymph nodes; (6) Low or absent NK-cell activity; (7) Ferritin greater than 500 ug/L; (8) Soluble IL-2 receptor (CD25) greater than 2400 U/mL. The treatment consists in a first step of trigger eradication (i.e., an underlying infectious agent) and then reducing the lymphocytes activation (steroids, etoposide, anti-T-cell agents, as well as new biologic treatments, and eventually allogenic stem cell transplantation).…”
Section: Introductionmentioning
confidence: 99%
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“…Clinical patterns range between signs and symptoms of sepsis, SIRS, shock and multi-organ failure [2]. Diagnosis is confirmed when at least 5 out of 8 criteria are met [3]: (1) fever; (2) Splenomegaly; (3) Cytopenias affecting 2 of 3 lineages in the peripheral blood: a) hemoglobin less than 90 g/L or less than 100 g/L in infants < 4 weeks; b) Platelets less than 100 x10 9 /L; c) Neutrophils less than 1.0 x 10 9 /L; (4) Hypertriglyceridemia and/or hypofibrinogenemia; (5) Hemophagocytosis in bone marrow, spleen or lymph nodes; (6) Low or absent NK-cell activity; (7) Ferritin greater than 500 ug/L; (8) Soluble IL-2 receptor (CD25) greater than 2400 U/mL. The treatment consists in a first step of trigger eradication (i.e., an underlying infectious agent) and then reducing the lymphocytes activation (steroids, etoposide, anti-T-cell agents, as well as new biologic treatments, and eventually allogenic stem cell transplantation).…”
Section: Introductionmentioning
confidence: 99%
“…HLH can be primary (related to particular kinds of genes and immunodeficiencies), either secondary to infections (with the most common agent be the Epstein-Barr virus) or rheumatologic conditions (namely MAS: Macrophage Activation Syndrome). Other described potential triggers to be mentioned are medications, surgery, and during this last period, the COVID-19 agent [4][5][6][7][8][9][10][11]. In fact, the recently defined Pediatric Inflammatory Multisystem Syndrome temporally associated with SARS-CoV-2 infection (PIMS-TS) is a life-threating disease affecting children, likely related to some COVID-19 exposure and close resembling HLH and/or MAS [5][6][7][8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%
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