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Polycythemia in an infant secondary to granulocyte transfusions
Olufolake Adisa1, Jeanne E Hendrickson, Courtney K Hopkins
1Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta, Division of Pediatric Hematology/Oncology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Insights
Granulocyte transfusions can help neutropenic children with infections. A case report highlights a rare risk: polycythemia in an infant after granulocyte transfusions, emphasizing the need for awareness of transfusion complications.
Area of Science:
- Pediatric Hematology
- Transfusion Medicine
- Immunology
Background:
- Granulocyte transfusions are used for neutropenic pediatric patients with severe infections.
- Established risks include febrile reactions, fluid overload, alloimmunization, and lung injury.
- Less recognized adverse effects warrant further investigation.
Observation:
- A case report details an infant diagnosed with familial hemophagocytic lymphohistiocytosis.
- The infant received four daily transfusions of apheresis-collected, steroid-stimulated donor granulocytes (20 ml/kg).
Findings:
- Following granulocyte transfusions, the infant developed polycythemia.
- Hemoglobin levels increased significantly during the transfusion period.
Implications:
- This case highlights a potential, less-recognized adverse effect of granulocyte transfusions.
- Expanded knowledge of transfusion risks aids in prompt recognition and management of complications.
- Clinicians should consider polycythemia as a potential complication in infants receiving granulocyte transfusions.
Abstract:
Granulocyte transfusions may be useful for neutropenic pediatric patients with refractory bacterial or fungal infections. Many potential adverse sequelae associated with granulocyte transfusions are well recognized, including febrile reactions, fluid overload, alloimmunization, and lung injury. Other potential adverse sequelae, however, are less well known. This case report describes an infant with familial hemophagocytic lymphohistiocytosis who developed polycythemia (hemoglobin 10-17.6 g/dl) following four daily transfusions of 20 ml/kg of apheresis collected, steroid stimulated donor granulocytes. Expanded knowledge of potential risks of transfused granulocytes will allow for rapid recognition of transfusion-related complications, should they occur.
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