Haemophagocytic lymphohistiocytosis (HLH) is a rare disease with high mortality. We report a one-month-old infant presented with fever, pancytopenia, liver derangement, coagulopathy, and was subsequently diagnosed to have HLH. No secondary cause could be identified after extensive workup. She developed multi-organ failure with severe lactic acidosis that was refractory to other treatment. Continuous renal replacement therapy successfully corrected her lactic acidosis. Our case highlights the importance of monitoring serum lactate level in critically ill patients with severe metabolic acidosis.
机构:
Columbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USAColumbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USA
Ammari, AN
Schulze, KF
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机构:
Columbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USAColumbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USA
机构:
Columbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USAColumbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USA
Ammari, AN
Schulze, KF
论文数: 0引用数: 0
h-index: 0
机构:
Columbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USAColumbia Univ Coll Phys & Surg, Dept Pediat, Div Neonatal Perinatal Med, New York, NY 10032 USA