| Literature DB >> 31708548 |
Takuya Suda1, Takeshi Zoshima2, Akari Takeji1, Yasunori Suzuki1, Ichiro Mizushima2, Kazunori Yamada3, Akikatsu Nakashima1, Akihiro Yachie4, Mitsuhiro Kawano2.
Abstract
Adult-onset Still's disease (AOSD) usually affects young adults. Some cases of elderly-onset Still's disease (EOSD) have been reported, but its clinical features are unclear. We herein report a 74-year-old woman who developed AOSD with macrophage activation syndrome (MAS). We also reviewed 24 previous EOSD cases in patients over 70 years old and compared the findings with overall AOSD. While the clinical features were similar between the two, including the presence of MAS, disseminated intravascular coagulation was more frequent in EOSD than in AOSD. Furthermore, despite a similar frequency of glucocorticoid use, immunosuppressants and biologics were less frequently administered in EOSD than in AOSD. This report highlights the fact that typical AOSD can develop in elderly patients with some characteristic features.Entities:
Keywords: Adult onset Still's disease; elderly; interleukin-18; macrophage activation syndrome
Year: 2019 PMID: 31708548 DOI: 10.2169/internalmedicine.3727-19
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271