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Atlantoaxial Subluxation and Syringomyelia in Down Syndrome: Report of One Case

唐氏症兒童的頸部寰樞椎間關節半脫位合併脊髓空洞症:一病例報告

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摘要


頸部之寰樞椎間關節不穩定(atlantoaxial instability)在唐氏症兒並非罕見,但因關節脫位而導致神經狀則不常見,而合併有脊髓空洞症(syringomyelia)又更少見了。吾等報告一名四歲唐氏症女童有一年斜頸(torticollis)的病史及三個月來漸進性運動退化,表現出運動失調(ataxia),四肢不全麻痺(quadriparesis),並因急性下腹脹、無法排尿而住院;理學檢查發現有膀胱膨脹,反射過強(hyperreflexia),兩腳踝有陣攣(ankle clonus)現象,以及出現兩側Babinski氏病徵頸部X光檢查發現寰樞椎間關節半脫位(subluxation)並有脊髓空洞症現象,經過導尿及膀胱復健,並予以頸部固定整直(orthosis),病人情況逐漸改善。

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並列摘要


Atlantoaxial instability is a relatively frequent finding in Down syndrome, but syringomyelia is a rare symptom. A four-year-old girl with Down syndrome was noted to have one year history of torticollis and progressive motor deterioration presenting with abnormal gait, ataxia or quadriparesis for the past three months. She was admitted because of acute urinary retention. Physical examination showed distended urinary bladder, hyperreflexia, bilateral ankle clonus and the existence of Babinski's signs. The x-ray films of the cervical spine showed widening between the joint space of atlas and odontoid processes. Magnetic resonance imaging revealed C1-C2 subluxation with syringomyelia. After bladder training and cervical orthosis, the symptoms improved.

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