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Secondary Hemophagocytic Lymphohistiocytosis and Autoimmune Cytopenias: Case Description and Review of the Literature

Hemophagocytic lymphohistocytosis (HLH) is a rare hyperinflammatory condition which may be primary or secondary to many diseases, including hematologic malignancies. Due to its life-threatening evolution, a timely diagnosis is paramount but challenging, since it relies on non-specific clinical and l...

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Detaylı Bibliyografya
Yayımlandı:J Clin Med
Asıl Yazarlar: Fattizzo, Bruno, Ferraresi, Marta, Giannotta, Juri Alessandro, Barcellini, Wilma
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2021
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7923749/
https://ncbi.nlm.nih.gov/pubmed/33672504
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm10040870
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