人源化抗人IL-6受体单克隆抗体对中庄-西村综合征的影响

F. Furukawa
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引用次数: 5

摘要

中约-西村综合征(NNS)是一种非常罕见的遗传性疾病,其发病于婴儿期,伴有腹股沟样皮疹,并伴有轻度发热和结节性红斑样皮肤疹。NNS的治疗仍在摸索中。最近我们遇到了一例皮质类固醇和人源化抗人IL-6受体单克隆抗体治疗的病例。结果发热、皮疹未得到充分改善,脂肪萎缩、关节挛缩等临床症状逐渐加重。我们在此报告这些药物的作用,并讨论新的治疗方向的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of a humanized anti-human IL-6 receptor monoclonal antibody on Nakajo-Nishimura syndrome
Nakajo-Nishimura syndrome (NNS) is a very rare hereditary disorder that has its onset in infancy with pernio-like skin rashes, and is accompanied by remittent fever and nodular erythema-like skin eruptions. The treatment of NNS is still under groping. Recently we encountered a case that was treated by corticosteroid and a humanized anti-human IL-6 receptor monoclonal antibody. As a result, the fever and skin rash was not improved sufficiently, and clinical symptoms of fat atrophy and joint contracture were gradually progressing. We herein report the effects of these agents and discuss the possibilities of new treatment direction.
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