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Histoplasmosis-Induced Hemophagocytic Lymphohistiocytosis in an Adult Patient: A Case Report and Review of the Literature

Hemophagocytic lymphohistiocytosis (HLH) is an aggressive and life-threating immune dysregulation syndrome characterized by persistent activation of the mononuclear phagocytic system leading to uncontrolled systemic hyperinflammatory response. The proliferation and activation of histiocytes and lymp...

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Detalles Bibliográficos
Autores principales: Untanu, Ramona Vesna, Akbar, Syed, Graziano, Stephen, Vajpayee, Neerja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088313/
https://www.ncbi.nlm.nih.gov/pubmed/27830097
http://dx.doi.org/10.1155/2016/1358742

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