Hemophagocytic lymphohistiocytosis in SARS-CoV-2 infection

A previously healthy 55-year-old woman presented with fever, malaise, and a mild cough. Chest radiograph revealed bilateral patchy infiltrates. A nasopharyngeal swab tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA. Progressive respiratory insufficiency necessitated intubation on admission day 3. She developed profound normocytic anemia (hemoglobin, 6.8 g/dL) and thrombocytopenia (23 3 103/mL) that were refractory to platelet and erythrocyte transfusions. Ferritin levels increased sharply, peaking at admission day 8 (19 558 ng/mL). Bone marrow examination revealed striking hemophagocytosis and erythroid hyperplasia. Hemophagocytosis refers to the pathologic finding of macrophage engulfment of host blood cells (panel A, engulfment of a granulocyte; panels B-F, engulfment of various erythroid precursors; panel G, engulfment of a megakaryocyte nucleus; all panels, original magnification 3100, May-Grünwald-Giemsa stain). There was no evidence of bacterial infection or hematological malignancy. The ensemble of bicytopenia, extreme hyperferritinemia, and hemophagocytosis, unexplained by other causes, yields a likely diagnosis of reactive hemophagocytic lymphohistiocytosis. Hydroxychloroquine was discontinued after cardiac arrhythmia provoked by severe pulmonary embolism. The clinical course was protracted; transfusion dependency abated, and the patient recovered after 45 days of ventilator dependency and supportive care.