Adult-onset Still’s disease in pregnancy complicated by macrophage activation syndrome
Abstract
Adult-onset Still’s disease is a rare polygenicautoinflammatory disease characterized by the classic triad of persistent high spiking fevers, joint pain (arthritis), and a distinctive salmon-colored bumpy rash. In the past decade, some pathophysiological mechanisms of the disease have been clarified and some sensitive and specific diagnostic criteria have been suggested. The disease is considered a diagnosis of exclusion. The course of the disease can be either relatively favorable or severe and disabling. Treatment is based on the use of glucocorticoids, immunosuppressive therapy and monoclonal antibodies. In the early 21 st century, descriptions of isolated cases and small series of adult-onset Still’s disease in pregnancy appeared in literature
About the Authors
N. I. Artishevskaia
Belarusian State Medical University
Belarus
Belarus
T. G. Rayeuneva
Belarusian State Medical University
Belarus
Belarus
S. E. Aliakseitshik
Belarusian State Medical University
Belarus
Belarus
E. A. Mikhnevich
The 3rdCity Clinical Hospital
Belarus
Belarus
A. M. Malyuta
The 3rdCity Clinical Hospital
Belarus
Belarus
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Review
For citations:
Artishevskaia N.I., Rayeuneva T.G., Aliakseitshik S.E., Mikhnevich E.A., Malyuta A.M. Adult-onset Still’s disease in pregnancy complicated by macrophage activation syndrome. Emergency Cardiology and Cardiovascular Risks journal. 2020;4(1):877–881. (In Russ.)
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