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Peripheral platelet phagocytosis in an extremely low birth weight infant: a case report

A 768 g female neonate, born at 25 weeks’ gestation, developed sepsis due to methicillin-resistant Staphylococcus epidermidis on day 14. Severe thrombocytopenia was observed, and hemophagocytic macrophages were identified in her peripheral blood smear. Cytokine profiles at the time of onset suggeste...

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Detalles Bibliográficos
Autores principales: Hatanaka, Daisuke, Ito, Kana, Fukama, Eisuke, Nomura, Tomoaki, Kusakari, Michiko, Takahashi, Hidehiro, Nakamura, Toshihiko, Takahashi, Naoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Fukushima Society of Medical Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493337/
https://www.ncbi.nlm.nih.gov/pubmed/35732414
http://dx.doi.org/10.5387/fms.2022-03
Descripción
Sumario:A 768 g female neonate, born at 25 weeks’ gestation, developed sepsis due to methicillin-resistant Staphylococcus epidermidis on day 14. Severe thrombocytopenia was observed, and hemophagocytic macrophages were identified in her peripheral blood smear. Cytokine profiles at the time of onset suggested that an inflammatory cytokine storm had activated lymphocytes and macrophages, leading to platelet phagocytosis. After administration of vancomycin for 14 days and immunoglobulin therapy, she improved without any complications. Considering the results of cytokine profiles, early intervention for infection may have prevented progression to hemophagocytic lymphohistiocytosis and reduced the severity of clinical symptoms.