Title of article :
Successful Recovery of a Child with COVID-19-Induced Secondary Hemophagocytic Lymphohistiocytosis
Author/Authors :
Mostafavi, Nassereddin Pediatric Department - School of Medicine -Isfahan University of Medical Sciences, Isfahan, Iran , Sadeghizadeh, Atefeh Pediatric Department - School of Medicine -Isfahan University of Medical Sciences, Isfahan, Iran , Babaei, Sharareh Pediatric Department - School of Medicine -Isfahan University of Medical Sciences, Isfahan, Iran , Saleh, Rana Pediatric Department - School of Medicine -Isfahan University of Medical Sciences, Isfahan, Iran , Dehghan, Amin Student Research Committee - School of Medicine - Isfahan University of Medical Sciences, Isfahan, Iran , Tavakoli, Saaman Pediatric Department - School of Medicine -Isfahan University of Medical Sciences, Isfahan, Iran , Pourmoghaddas, Zahra Pediatric Department - School of Medicine -Isfahan University of Medical Sciences, Isfahan, Iran
Abstract :
The coronavirus disease 2019 (COVID-19) pandemic has imposed a significant burden worldwide, manifesting as a severe disease and causing mortality even in children. Severe COVID-19 disease is characterized by cytokine storm with progression to secondary
hemophagocytic lymphohistiocytosis (sHLH). We describe an 18-month-old boy in Iran, previously healthy, diagnosed with COVID19-induced sHLH. Three weeks after close contact with COVID-19 confirmed cases, he was admitted with high fever, lethargy, mild respiratory distress, skin rash, and conjunctivitis with swollen eyelids and lips. Laboratory data revealed elevated levels of erythrocyte
sedimentation rate (ESR), C-reactive protein (CRP) and liver enzymes, and mild thrombocytopenia. His clinical condition rapidly
deteriorated, with septic shock, hepatosplenomegaly, and respiratory failure. Laboratory tests showed cytopenia, coagulopathy, hyperferritinemia, and hypertriglyceridemia, which met the criteria for sHLH diagnosis. Chest computed tomography (CT) revealed
bilateral infiltrations that suggested acute respiratory distress syndrome (ARDS) of COVID-19 that was confirmed by a positive realtime polymerase chain reaction (RT-PCR) test. Therefore, the child was treated with intravenous immunoglobulin (IVIG), glucocorticoid, hydroxychloroquine, lopinavir/ritonavir, and interferonβ-1a. This therapeutic strategy enabled complete recovery from fever,
regaining consciousness, weaning from respiratory support, and resolving shock. Serial chest radiographs showed diminishing
infiltrations. Sequential physical examinations revealed an overall significant reduction in spleen and liver span. Laboratory data
showed rapid improvement from cytopenia and coagulopathy, normalization of liver enzyme levels, and reduction in hyperinflammation markers. Although ARDS is the most common cause of death from COVID-19, other complications such as sHLH may be
lethal; thus, early diagnosis and appropriate treatment are necessary for saving patients’ lives
Keywords :
COVID-19 , Children , Hemophagocytic Lymphohistiocytosis
Journal title :
Archives of Pediatric Infectious Diseases