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Hemophagocytic Lymphohistiocytosis (HLH) in a Patient with Disseminated Histoplasmosis

Hemophagocytic lymphohistiocytosis (HLH) is a rare condition characterized by an overwhelming inflammatory cascade activation which is often associated with rapid progression and high mortality. It may be familial with an underlying genetic mutation or triggered by infection, malignancy, and autoimm...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Case Rep Hematol
Hauptverfasser: Swaminathan, Neeraja, Vinicius, Jorge M., Serrins, Jesse
Format: Artigo
Sprache:Inglês
Veröffentlicht: Hindawi 2020
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7387958/
https://ncbi.nlm.nih.gov/pubmed/32765915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/5638262
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