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A Case of Hemophagocytic Lymphohistiocytosis Presenting with Neck Mass in a Child / 대한두경부종양학회지
Korean Journal of Head and Neck Oncology ; (2): 55-59, 2020.
Article Dans Coréen | WPRIM | ID: wpr-894405
ABSTRACT
Hemophagocytic lymphohistiocytosis (HLH) is a rare but life-threatening one syndrome of excessive immune activation. This immune dysregulation disorder is prominently associated with cytopenias and combinations of clinical signs and extreme inflammation symptoms. For survival, it is important to diagnose early and treat appropriately. We report a case of 10 years old boy who was admitted to the hospital with a month history of fever and cervical lymph node enlargement. There were signs of hemophagocytic histiocytosis in the lymph node and bone marrow. The etiology, diagnosis, and treatment of hemophagocytic lymphohistiocytosis are reviewed.
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) langue: Coréen Texte intégral: Korean Journal of Head and Neck Oncology Année: 2020 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) langue: Coréen Texte intégral: Korean Journal of Head and Neck Oncology Année: 2020 Type: Article