Spasmodic torticollis possibly secondary to a vertebral hemangioma

被引:7
作者
Durán, E [1 ]
Chacón, JR [1 ]
机构
[1] Univ Seville, Hosp Virgen Macarena, Serv Neurol, E-41071 Seville, Spain
关键词
dystonia; hemangioma; motor-neurone; spinal cord; torticollis; vertebral disorders;
D O I
10.33588/rn.3201.99614
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction. Spasmodic torticollis in young patients should give rise to a clinical suspicion that this is secondary to another primary disorder. Therefore a series of diagnostic tests should be carried out before it is labelled as idiopathic. Clinical case. The patient was a thirty year old man who had had difficulty in writing with his right hand since childhood At the age of 20 years he was diagnosed as having writer's cramp and idiopathic spasmodic torticollis. On general physical examination no abnormalities,were found. On neurological examination he had absence of reflexes of both arms, limited but painless rotation of the neck towards the left and hypertrophy of the left trapezius muscle. Laboratory, neurophysiological and neuroimaging investigations seeking a secondary cause for the torticollis were all normal. There were no Keyser-Fleischer rings. Chest X-ray showed dorsal scoliosis,with convexity to the left. CAT and MR of the spine show ed a hemangioma in the body of T-1. On arteriography of the supra-aortic and vertebral trunks a hemangioma was found at T-1 which received contrast material via a branch of the right thyro-bicervicoscapular trunk. Various treatments were tried (diazepam, Botox (R) Dysport (R), tetrabenazine, baclofen, etc.) with no improvement. A definite diagnosis of secondary torticollis could not be mane since the hemangioma was supplied by a very narrow vascular pedicle, so embolization was contraindicated. Conclusion. Cervical spinal cord alterations may cause focal dystonia die to increased excitability of the spinal motor neurone, due to dysfunction of the desinhibitory descending reciprocal paths.
引用
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页码:60 / 62
页数:3
相关论文
共 17 条
[1]   DYSTONIA OF THE LEGS INDUCED BY WALKING OR PASSIVE MOVEMENT OF THE BIG TOE IN A PATIENT WITH CEREBELLAR ECTOPIA AND SYRINGOMYELIA [J].
BERARDELLI, A ;
THOMPSON, PD ;
DAY, BL ;
ROTHWELL, JC ;
OBRIEN, MD ;
MARSDEN, CD .
NEUROLOGY, 1986, 36 (01) :40-44
[2]   The pathophysiology of primary dystonia [J].
Berardelli, A ;
Rothwell, JC ;
Hallett, M ;
Thompson, PD ;
Manfredi, M ;
Marsden, CD .
BRAIN, 1998, 121 :1195-1212
[3]   CERVICAL DYSTONIA DUE TO SPINAL-CORD EPENDYMOMA - INVOLVEMENT OF CERVICAL CORD SEGMENTS IN THE PATHOGENESIS OF DYSTONIA [J].
CAMMAROTA, A ;
GERSHANIK, OS ;
GARCIA, S ;
LERA, G .
MOVEMENT DISORDERS, 1995, 10 (04) :500-503
[5]  
Jabbari B, 1999, MOVEMENT DISORD, V14, P860, DOI 10.1002/1531-8257(199909)14:5<860::AID-MDS1024>3.0.CO
[6]  
2-8
[7]   TORTICOLLIS IN 3 CHILDREN WITH SYRINGOMYELIA AND SPINAL-CORD TUMOR [J].
KIWAK, KJ ;
DERAY, MJ ;
SHIELDS, WD .
NEUROLOGY, 1983, 33 (07) :946-948
[8]  
KOSTERMANN W, 1993, MOVEMENT DISORD, V8, P234
[9]   DYSTONIA FOLLOWING HEAD TRAUMA - A REPORT OF 9 PATIENTS AND REVIEW OF THE LITERATURE [J].
KRAUSS, JK ;
MOHADJER, M ;
BRAUS, DF ;
WAKHLOO, AK ;
NOBBE, F ;
MUNDINGER, F .
MOVEMENT DISORDERS, 1992, 7 (03) :263-272
[10]  
MADHUSUDANAN M, 1995, ACTA NEUROL SCAND, V92, P308