Literature DB >> 8153810

Juvenile compression myelopathy in the cervical spine.

H Okumura1, T T Homma.   

Abstract

Juvenile-type distal muscular atrophy of the upper extremities is a condition characterized by juvenile onset, muscular atrophy limited to the hand and forearm, and lack of definite sensory disturbance. Diagnostic imaging techniques and operative findings showed compressive lesions of the cervical spinal cord in seven cases showing distal muscular atrophy of the upper extremities. In most of these cases, cord compression could be recognized, not during neck extension, but during flexion on myelogram, computed tomography, and magnetic resonance imaging. All cases underwent anterior spinal fusion to prevent flexion at the affected site, and the dural tube was opened to observe the surface of the cervical cord in four cases. It was confirmed that cervical myelopathy can occur even in young persons with no spondylotic change in the cervical spine.

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Year:  1994        PMID: 8153810     DOI: 10.1097/00007632-199401000-00016

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  2 in total

1.  Cervical spondylotic amyotrophy: a systematic review.

Authors:  Wenqi Luo; Yueying Li; Qinli Xu; Rui Gu; Jianhui Zhao
Journal:  Eur Spine J       Date:  2019-04-29       Impact factor: 3.134

2.  Electrophysiological differences between Hirayama disease, amyotrophic lateral sclerosis and cervical spondylotic amyotrophy.

Authors:  Xiang Jin; Jian-Yuan Jiang; Fei-Zhou Lu; Xin-Lei Xia; Li-Xun Wang; Chao-Jun Zheng
Journal:  BMC Musculoskelet Disord       Date:  2014-10-16       Impact factor: 2.362

  2 in total

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