Abstract
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.
Original language | English |
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Pages (from-to) | 442-444 |
Number of pages | 3 |
Journal | Netherlands Journal of Medicine |
Volume | 76 |
Issue number | 10 |
Publication status | Published - 2018 Dec |
All Science Journal Classification (ASJC) codes
- Internal Medicine