Journal of Pediatric Hematology/Oncology · 2011 · 16 citations · 14 references
MedicineHematologyOncologyChemotherapyHematopathologyPediatric HematologyBone Marrow PathologyHematologic DisordersHematologic MalignanciesHematologic PathologyHematopoietic NeoplasmsPediatric HematopathologyAcute Lymphoblastic Leukemia TreatmentB-cell Acute Lymphoblastic LeukemiaB-cell LeukemiaHematologic Malignancy-associated InfectionsHemophagocytosis In Bone MarrowLeukemia PathologyParvovirus B19 Infection DiagnosisProlonged Cytopenia
Development of hemophagocytic lymphohistiocytosis (HLH) is quite rare among acute lymphoblastic leukemia (ALL) patients. We present a 3-year-old boy with precursor B-cell ALL, who was complicated by HLH because of parvovirus B19 infection during maintenance chemotherapy. Remarkable erythroid hypoplasia, giant normoblasts, and hemophagocytosed macrophages in bone marrow were important clues for the diagnosis. The patient was successfully treated with high-dose steroids and intravenous immunoglobulins. To our knowledge, this is the first report describing parvovirus B19-associated HLH in ALL. Our case highlights that parvovirus B19 can cause HLH, a potentially fatal disorder, and prolonged unexpected cytopenia in childhood ALL.
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HLH‐2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
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