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...

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Detaylı Bibliyografya
Yayımlandı:Case Rep Hematol
Asıl Yazarlar: Swaminathan, Neeraja, Vinicius, Jorge M., Serrins, Jesse
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2020
Konular:
Case Report
Online Erişim: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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