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自发性肩关节后脱位作为夏科关节病的首发症状。

Spontaneous posterior shoulder dislocation as the first symptom of a Charcot arthropathy.

作者信息

Hernigou Jacques, Boulares Sofiane, Delahaut Olivier

出版信息

Acta Orthop Belg. 2018 Mar;84(1):73-77.

PMID:30457503
Abstract

Neuroarthropathy or Charcot disease is a destructive joint pathology. Upper limb involvement is unusual and often due to syringomyelia. We reported a patient with spontaneous posterior right shoulder dislocation. Thereafter, she presented a quick joint destruction evoking a Charcot shoulder disease after excluding infectious and rheumatologic diseases. Explorations of this Charcot disease lead to the discovery and treatment of syringomyelia. A conservative management of her shoulder neuro-arthropathy has been proposed to the patient. Shoulder involvement in Charcot disease is unusual: only 5% of cases. 18 cases have been reported in English literature. Two theories try to explain Charcot disease: neuro-vascular and neuro-traumatic. There is no efficient treatment for Charcot shoulder disease but it can be prevented by surgical treatment of syringomyelia. Charcot shoulder is a rare and morbid disease for which conservative treatment is recommended because of disappointing results of arthroplasty and arthrodesis.

摘要

神经性关节病或夏科氏病是一种破坏性关节病变。上肢受累情况不常见,且往往由脊髓空洞症引起。我们报告了一例自发性右肩关节后脱位患者。此后,在排除感染性和风湿性疾病后,她迅速出现关节破坏,引发了夏科氏肩关节病。对该夏科氏病的检查发现并治疗了脊髓空洞症。已向患者提出对其肩部神经性关节病进行保守治疗。夏科氏病累及肩部的情况不常见:仅占病例的5%。英文文献中已报道了18例。有两种理论试图解释夏科氏病:神经血管学说和神经创伤学说。对于夏科氏肩关节病尚无有效的治疗方法,但可通过脊髓空洞症的手术治疗来预防。夏科氏肩关节病是一种罕见且病情严重的疾病,由于关节成形术和关节融合术效果不佳,建议采用保守治疗。

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引用本文的文献

1
Neuropathic arthropathy of the shoulder secondary to operated syringomyelia: a case-based review.手术治疗后脊髓空洞症继发肩部神经性关节病:病例回顾
Rheumatol Int. 2023 Apr;43(4):777-790. doi: 10.1007/s00296-022-05234-w. Epub 2022 Oct 22.
2
Neuropathic arthropathy of the shoulder as a presenting feature of Chiari malformation with syringomyelia: a case report with a systematic literature review.以 Chiari 畸形伴脊髓空洞症为表现的肩部神经关节病:病例报告及系统文献复习。
Eur Spine J. 2022 Oct;31(10):2733-2752. doi: 10.1007/s00586-022-07299-4. Epub 2022 Jul 16.