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Published on: May 26, 2023
Corticosteroid treatment in patients with Sydenham's chorea
Judith Barash1, Dov Margalith, Abraham Matitiau
1Pediatric Rheumatology, Kaplan Medical Center, Rehovot 76100, Israel.
Insights
Corticosteroids rapidly resolved Sydenham's chorea symptoms in five pediatric patients, offering a potential new treatment for this acute rheumatic fever complication. This approach showed no relapses, suggesting its efficacy for involuntary movement disorders.
Area of Science:
- Pediatric Neurology
- Rheumatology
- Immunology
Background:
- Sydenham's chorea is a significant manifestation of acute rheumatic fever, characterized by involuntary movements.
- Current treatment primarily involves supportive care, with a high risk of recurrence.
- The underlying pathophysiology involves autoimmune responses targeting the basal ganglia.
Observation:
- Five pediatric patients with Sydenham's chorea were treated with a short course of corticosteroids.
- Involuntary movements showed marked improvement within 24-48 hours of treatment initiation.
- Complete resolution of symptoms was observed within 7-12 days.
Findings:
- Corticosteroid therapy led to rapid and complete resolution of choreiform movements.
- No relapses were reported during the observation period following treatment.
- This suggests a potential therapeutic benefit of corticosteroids in managing Sydenham's chorea.
Implications:
- Corticosteroids may offer an effective treatment option for Sydenham's chorea, reducing disease duration and recurrence risk.
- Further research, including larger comparative studies, is warranted to confirm these findings.
- This approach could significantly improve patient outcomes for this debilitating neurological condition.
Abstract:
Sydenham's chorea occurs in approximately 10% of acute rheumatic fever and is one of its major manifestations. The disease may last for weeks or months, with a high risk of recurrence; usually only supportive treatment is recommended. This report describes five children diagnosed with Sydenham's chorea and treated with a short course of corticosteroids. Marked improvement of the involuntary movements was observed within 24-48 hours, with complete resolution within 7-12 days after commencement of treatment; there were no relapses. Larger, possibly comparative studies are necessary, but in the meantime treatment with corticosteroids in patients with Sydenham's chorea should be considered.
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