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 |
|---|---|
| Pages (from-to) | 1155-1161 |
| Number of pages | 7 |
| Journal | Indian Pediatrics |
| Volume | 58 |
| Issue number | 12 |
| Early online date | 26 Mar 2021 |
| DOIs | |
| Publication status | Published - 15 Dec 2021 |
Keywords
- Child
- Humans
- Lymphohistiocytosis, Hemophagocytic/diagnosis
- Macrophage Activation Syndrome/diagnosis