Results 1 to 10 of about 22,345 (254)

An analysis of reported cases of hemophagocytic lymphohistiocytosis (HLH) after COVID-19 vaccination

open access: yesHuman Vaccines and Immunotherapeutics, 2023
Although COVID-19 vaccines are an effective public health tool to combat the global pandemic, serious adverse events, such as hemophagocytic lymphohistiocytosis (HLH), caused by them are a concern.
Qing-Tai Cao, Marady Hun, Lin Cao
exaly   +2 more sources

CNS Involvement in HLH (CNS-HLH)

open access: yes, 2017
CNS disease is considered to be a result of the pathologic immune response in HLH. CNS involvement is frequently found at diagnosis or can occur anytime in the further course of systemic HLH but has also been reported as primary or only manifestation.
AnnaCarin Horne, Karin Beutel
openaire   +2 more sources

Early imaging differentiation of children with acute hematologic malignancies that present in pancytopenia: a retrospective study [PDF]

open access: yesFrontiers in Oncology
ObjectivesThis retrospective cohort study aimed to identify potential differentiation indicators on thoracic and abdominal computed tomography (CT) among three hematologic malignancies characterized by acute pancytopenia in children.MethodsThis study was
Junya Ma   +8 more
doaj   +2 more sources

Transcriptional Targets of the REF-1 Family Proteins: HLH-25/ HLH-28/HLH-29

open access: yes, 2011
Notch signaling is important for development in Caenorhabditis elegans and the REF-1 family pro-teins, a set of the bHLH transcription factors, are the first targets of Notch signaling. Little is known about the molecular mechanisms employed by the REF-1 family to regulate development.
Wang, Kun
openaire   +3 more sources

Identifying Hemophagocytic Lymphohistiocytosis and Describing Outcomes Using Computable Phenotypes: Retrospective Cohort Study [PDF]

open access: yesJMIR Cancer
BackgroundHemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome that requires rapid diagnosis and intervention. However, identifying these patients is difficult because the HLH-2004 diagnostic criteria are complex and ...
Suheyla Ocak   +7 more
doaj   +2 more sources

Hemophagocytic Lymphohistiocytosis (HLH)

open access: yesSouth Eastern European Journal of Public Health
HLH is a reactive process resulting from prolonged and excessive antigen-presenting cell activation [1]. Hemophagocytosis is a hallmark of activated macrophages/histiocytes. The predominant clinical findings of HLH are fever (often hectic and persistent), cytopenia, hepatitis, and splenomegaly. A case of HLH in a 32-year-old female with no past medical
Fadi Mohammad Mobarrak, Farid Ullah Khan
core   +4 more sources

Adult-onset primary hemophagocytic syndrome with concurrent Epstein–Barr virus infection: a case report with literature review [PDF]

open access: yesFrontiers in Oncology
ObjectiveTo investigate the clinical and laboratory features, phenotypic characteristics, associated genes, and treatment strategies for adult primary hemophagocytic lymphohistiocytosis (HLH).MethodsThe clinical characteristics and underlying causes of ...
Lei Huang, Shuli Guo
doaj   +2 more sources

Real-world use of emapalumab in hemophagocytic lymphohistiocytosis: a scoping review of published evidence [PDF]

open access: yesFrontiers in Pharmacology
BackgroundEmapalumab, an interferon-γ (interferon-gamma)–blocking monoclonal antibody, has emerged as a targeted therapy for refractory hemophagocytic lymphohistiocytosis (HLH).
Abdulrahman F. Al-Mashdali   +7 more
doaj   +2 more sources

A Wolf in Sheep's Clothing: Systemic Immune Activation Post Immunotherapy [PDF]

open access: yesJournal of Immunotherapy and Precision Oncology, 2021
Introduction: Immune checkpoint inhibitors (ICIs) are increasingly a standard of care for many cancers; these agents can result in immune-related adverse events (irAEs) including fever, which is common but can rarely be associated with systemic immune ...
Crescens Tiu   +14 more
doaj   +1 more source

A Rare Initial Presentation in Extra Pulmonary Tuberculosis- Hemophagocytic Lymphohistiocytosis as a Differential Diagnosis

open access: yesSri Lanka Journal of Medicine, 2022
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder characterized by excessive activation of the immune system leading to tissue damage and organ dysfunction.
U. P. Edirisinghe, J. Indrakumar
doaj   +1 more source

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