Spinal pseudoathetosis: a rare, forgotten syndrome, with a review of old and recent descriptions.
Détails
ID Serval
serval:BIB_3FE4F442D0D6
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Spinal pseudoathetosis: a rare, forgotten syndrome, with a review of old and recent descriptions.
Périodique
Neurology
ISSN
0028-3878 (Print)
ISSN-L
0028-3878
Statut éditorial
Publié
Date de publication
1997
Volume
49
Numéro
2
Pages
432-437
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
We report a patient with a cervical spinal astrocytoma who presented with athetotic hand movements. We postulate that acute pain, related to a syrinx around the operative site, contributed to the athetosis. These movements occur only after protracted, severe loss of proprioception, often in conjunction with an acute, generally painful crisis. Athetotic movements can disappear without change in proprioceptive or motor deficits when pain lessens.
Mots-clé
Adult, Astrocytoma/complications, Astrocytoma/surgery, Athetosis/diagnosis, Athetosis/etiology, Electromyography, Humans, Magnetic Resonance Imaging, Pain, Postoperative Complications, Proprioception, Radiosurgery, Spinal Cord Diseases/diagnosis, Spinal Cord Diseases/etiology, Spinal Cord Neoplasms/complications, Spinal Cord Neoplasms/surgery, Syringomyelia/complications, Syringomyelia/physiopathology
Pubmed
Web of science
Création de la notice
25/01/2008 11:45
Dernière modification de la notice
20/08/2019 13:37