Hemophagocytic Lymphohistiocytosis Secondary to Bone Marrow Only B-Cell Lymphoma: A Very Rare Entity With an Even Rarer Presentation

Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome. It is categorized as familial or acquired, most commonly caused by infections, malignancies, rheumatologic and immunodeficiency disorders. Irrespective of the etiology, the age at the onset is the strongest prognostic fac...

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Detalles Bibliográficos
Autores principales: Patel, Ami, Vakiti, Anusha, Chilkulwar, Abhishek, Mewawalla, Prerna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155825/
https://www.ncbi.nlm.nih.gov/pubmed/32300392
http://dx.doi.org/10.14740/jh324w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155825/
https://www.ncbi.nlm.nih.gov/pubmed/32300392
http://dx.doi.org/10.14740/jh324w

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