[A case of Stiff-person syndrome with muscle tonicity of the extremities and neck after use of Dulvalumab for lung adenocarcinoma].

Q4 Medicine Clinical Neurology Pub Date : 2024-03-22 Epub Date: 2024-02-17 DOI:10.5692/clinicalneurol.cn-001923
Takashi Inoue, Kei Oiwa, Kazuhiro Horiuchi
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Abstract

A 74-year-old woman taking dulvalumab for lung adenocarcinoma developed muscle tonicity in the extremities and trunk. Painful paroxysmal muscle spasms with profuse sweating were frequently observed, and surface electromyography showed simultaneous contraction of the active and antagonist muscles. Blood tests were strongly positive for anti-amphiphysin antibodies, and stiff-person syndrome (SPS) was diagnosed. Intravenous immunoglobulin therapy and clonazepam were initiated, and the paroxysmal painful muscle spasms disappeared. As the primary tumor was under control, and the onset occurred approximately six weeks after the resumption of immune checkpoint inhibitors, we considered SPS to be an immune-related adverse event. Although extremely rare, it should be considered a neuromuscular disease that can occur in association with immune checkpoint inhibitors.

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[肺腺癌患者使用度维单抗后出现四肢和颈部肌肉强直的僵人综合征病例]。
一名 74 岁的妇女因肺部腺癌服用度维单抗后,出现四肢和躯干肌肉强直。经常出现阵发性疼痛性肌肉痉挛,伴有大量出汗,表面肌电图显示主动肌和拮抗肌同时收缩。血液化验结果显示抗虹膜蛋白抗体呈强阳性,诊断为僵人综合征(SPS)。开始静脉注射免疫球蛋白和氯硝西泮,阵发性疼痛性肌肉痉挛消失了。由于原发性肿瘤已得到控制,且发病发生在恢复使用免疫检查点抑制剂约六周后,我们认为SPS是一种免疫相关不良事件。尽管这种情况极为罕见,但应将其视为与免疫检查点抑制剂相关的神经肌肉疾病。
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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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