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系统性韦格纳-克里斯蒂安病并发部分横贯性脊髓病。

Systemic Weber-Christian disease complicated by partial transverse myelopathy.

作者信息

Larner A J, Marshall B, Ma R C, Ball J A

机构信息

Department of Neurology, St Mary's Hospital, London, UK.

出版信息

Int J Clin Pract. 2000 Sep;54(7):472-4.

Abstract

Weber-Christian disease is an inflammatory disorder of fatty tissue which usually presents with raised red tender nodules in the skin. Although there may be additional systemic upset, there are very few reports of neurological features associated with this condition. We report a patient with biopsy-confirmed systemic Weber-Christian disease in whom a transient partial myelopathy, of probable inflammatory origin, was the most prominent feature. Based on recent reports of the effects of immune mediators on neuronal function, a possible pathogenetic explanation for this syndrome is suggested.

摘要

韦格纳-克里斯蒂安病是一种脂肪组织的炎症性疾病,通常表现为皮肤出现红色、压痛性隆起结节。虽然可能会有其他全身不适症状,但与该疾病相关的神经学特征的报道非常少。我们报告一例经活检确诊为系统性韦格纳-克里斯蒂安病的患者,其最突出的特征是可能由炎症引起的短暂性部分脊髓病。基于近期关于免疫介质对神经元功能影响的报道,提出了该综合征可能的发病机制解释。

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