Abstract
Macrophage activation syndrome is a severe yet under-recognized complication encountered in pediatric rheumatology. It manifests as secondary hemophagocytic lymphohistiocytosis leading to a hyper-inflammatory state resulting from an underlying cytokine storm. If unchecked, it may lead to multiorgan failure and mortality. Early diagnosis and timely initiation of specific therapy is pivotal for a successful outcome. This review outlines the key clinical and laboratory features and management of macrophage activation syndrome.
Original language | English |
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Pages (from-to) | 1155-1161 |
Number of pages | 7 |
Journal | Indian pediatrics |
Volume | 58 |
Issue number | 12 |
DOIs | |
Publication status | Published - 15 Dec 2021 |
Keywords
- Child
- Humans
- Lymphohistiocytosis, Hemophagocytic/diagnosis
- Macrophage Activation Syndrome/diagnosis