继发于脊髓空洞症的神经性胸锁关节。病例报告。
Neuropathic sternoclavicular joint secondary to syringomyelia. A case report.
作者信息
Chidgey L K, Szabo R M, Benson D R
机构信息
Department of Orthopedic Surgery, University of California, Davis, Sacramento 95817.
出版信息
Orthopedics. 1988 Nov;11(11):1571-3. doi: 10.3928/0147-7447-19881101-11.
PMID:3200768
Abstract
A 14-year-old boy is presented with syringomyelia and a neuropathic sternoclavicular joint. Recognition of neuropathic arthropathy of the upper extremity is important when a massive, destructive joint lesion exists in a patient with syringomyelia.
摘要
一名14岁男孩患有脊髓空洞症和神经性胸锁关节病。当脊髓空洞症患者出现巨大的、破坏性的关节病变时，认识到上肢的神经性关节病很重要。
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