Hemophagocytic lymph histiocytosis (HLH): etiologies, pathogenesis, treatment, and outcomes in critically ill patients: a review article and literature to review

Hemophagocytic lymph histiocytosis (HLH) is not an independent disease but is instead a clinical syndrome that occurs in many underlying conditions involving all age groups. HLH is the consequence of a severe, uncontrolled hyperinflammatory reaction that in most cases is triggered by an infectious a...

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Bibliographic Details
Main Authors: Mohsin Mirza, Maryam Zafar, Joseph Nahas, Wafa Arshad, Anum Abbas, Abubakar Tauseef
Format: Article
Language:English
Published: Greater Baltimore Medical Center 2021-09-01
Series:Journal of Community Hospital Internal Medicine Perspectives
Subjects:
Online Access:http://dx.doi.org/10.1080/20009666.2021.1954783