Hemophagocytic lymphohistiocytosis (HLH) is a rapidly progressing, life-threatening
syndrome characterized by excessive immune activation, often presenting as a complex …

Hemophagocytic lymphohistiocytosis (HLH) is a rare genetic hyperinflammatory syndrome
that occurs early in life. Macrophage activation syndrome (MAS) usually refers to a …

Primary hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder associated
with autosomal recessive variants in genes required for perforin-mediated lymphocyte …

Purpose GATA2 deficiency is an autosomal dominant disease that manifests with a range of
clinical symptoms, including increased susceptibility to viral, bacterial, and fungal infections …

Background Tuberculosis-associated hemophagocytic lymphohistiocytosis (TB-HLH)
presents significant challenges in diagnosis and treatment due to its complex interplay …

Hemophagocytic lymphohistiocytosis (HLH) is a common and highly fatal hyperinflammatory
syndrome characterized by the aberrant activation of macrophages. To date, there is a lack …

Managing acute myeloid leukemia (AML) and its critical complications requires
understanding the complex interplay between disease biology, treatment strategies, and …

Introduction: Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening syndrome
characterized by an uncontrolled hyperinflammatory reaction. HLH is classified into primary …

The development of anti-SARS-CoV-2 vaccines will stay as a landmark in the history of
modern medicine, both as a major scientific achievement and an unprecedented public …

Macrophage activation syndrome (MAS) is potentially fatal; so, early diagnosis and timely
treatment are essential. However, detecting MAS is sometimes challenging because its …