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Abstract: Macrophage activation syndrome (MAS) is a rare but serious immunological emergency often associated with chronic inflammatory diseases. It represents a secondary form of hemophagocytic lymphohistiocytosis (HLH) and is characterized by uncontrolled immune system activation. We report here two clinical cases identified within a biological hematology laboratory, illustrating the varied presentations, diagnostic challenges, biological features, and multidisciplinary management of MAS. DOI: http://dx.doi.org/10.51505/ijmshr.2025.9308 |
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