Adult-onset Still’s disease (AOSD) can progress into macrophage activation syndrome (MAS), which may be fatal. We report on a 19-year-old Han Chinese female, who presented with MAS-related pulmonary parenchymal involvement complicating AOSD, and further associated with disseminated intravascular coagulation and generalized tonic-clonic seizure. She was managed by high-dose corticosteroids and pulse cyclophosphamide therapy with a complete recovery of disease activity.
|頁（從 - 到）||442-444|
|期刊||Netherlands Journal of Medicine|
|出版狀態||Published - 2018 十二月|
All Science Journal Classification (ASJC) codes
- Internal Medicine