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Reversible propriospinal myoclonus due to thoracic disc herniation: long-term follow-up
Wooyoung Jang1, Joong-Seok Kim, Jin Young Ahn
1Department of Neurology, Hanyang University, College of Medicine, Seoul, Republic of Korea.
Abstract:
PSM is a rare form of myoclonus of spinal origin. The thoracic level is considered as the myoclonic generator in most cases; however, structural abnormality in conventional magnetic resonance imaging (MRI) related to PSM is more rare. We report the case of a 23-year-old man with PSM with ventral thoracic disc herniation confirmed by conventional MRI, which completely resolved after thoracic discectomy. This case indicates that decompressive surgery might be a valid treatment option.
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