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Refractory Autoimmune Hemophagocytic Lymphohistiocytosis in Adults: Multi-therapy Failure and the Limits of Salvage Transplantation. [PDF]
CureusAlmaalouli B +4 more
europepmc +1 more source
Clinical spectrum and laboratory correlates of concurrent hemophagocytic lymphohistiocytosis and toxoplasmosis: a systematic review. [PDF]
BMC Infect DisShahini A, Javan ZH, Ghasemikhah R.
europepmc +1 more source
An Unusual Presentation of Secondary Hemophagocytic Lymphohistiocytosis With Melena: A Case Report. [PDF]
CureusKant S +4 more
europepmc +1 more source
Hemophagocytic lymphohistiocytosis induced by radio-chemo-immunotherapy: a case report. [PDF]
Strahlenther OnkolSalazar-Zuniga B +5 more
europepmc +1 more source
Adult-Onset Still's Disease and Secondary Hemophagocytic Lymphohistiocytosis: Diagnostic Pitfalls in Lymph Node Histology. [PDF]
Iran J PatholMitra S, Nagpure K.
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Hemophagocytic Lymphohistiocytosis [PDF]
Annual Review of Pathology: Mechanisms of Disease, 2018 Hemophagocytic lymphohistiocytosis (HLH) is a rare syndrome of widespread inflammation due to massive amounts of cytokines released from activated macrophages. The most common trigger for HLH is infection from a virus, most commonly Epstein-Barr virus. Here we report an adult case of this rare and life-threatening syndrome.
Hanny Al-Samkari
exaly +5 more sources
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Hemophagocytic lymphohistiocytosis
The Indian Journal of Pediatrics, 1999Hemophagocytic lymphohistiocytosis (HLH) is a rare condition in children associated with immunodeficiency, life threatening infections and malignancy. Infection associated hemophagocytosis responds well to appropriate antimicrobioal therapy and rarely to steroids when the infective agent is suspected to be of viral origin.
N, Biswal +4 more
openaire +4 more sources