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Hemophagocytic lymphohistiocytosis and myelodysplastic syndrome: a case report and review of the literature

BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is characterized by hyperinflammation and life-threatening cytopenias. Survival is poor, and management is pivotal on rapid identification of the disease. HLH is associated with hematologic malignancies, however correlation with myelodysplastic sy...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Med Case Rep
Prif Awduron: Sun, Y., Blieden, C., Merritt, B. Y., Sosa, R., Rivero, Gustavo
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2021
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7919086/
https://ncbi.nlm.nih.gov/pubmed/33648567
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-020-02623-2
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