Hemophagocytic Lymphohistiocytosis in a Patient with Classical Hodgkin Lymphoma

Introduction. Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome that can be associated with inherited genetic mutations, malignancy, autoimmune disorders, and viral infections. Though the pathogenesis is not fully known, HLH is understood to be a reactive process in the s...

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Detalles Bibliográficos
Autores principales: Hyun, G., Robbins, K. J., Wilgus, N., Grosso, L., Goyal, S. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075614/
https://www.ncbi.nlm.nih.gov/pubmed/27803821
http://dx.doi.org/10.1155/2016/2103612

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075614/
https://www.ncbi.nlm.nih.gov/pubmed/27803821
http://dx.doi.org/10.1155/2016/2103612

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