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伊匹单抗治疗后与自身免疫性甲状腺炎相关的类固醇反应性脑病:一例报告

Steroid responsive encephalopathy associated with autoimmune thyroiditis following ipilimumab therapy: a case report.

作者信息

Carl David, Grüllich Carsten, Hering Steffen, Schabet Martin

机构信息

Department of Neurology, Klinikum Ludwigsburg, Posilipostraße 4, Ludwigsburg, Germany.

National Cent Tumor Diseases (NCT), Heidelberg, Germany.

出版信息

BMC Res Notes. 2015 Jul 26;8:316. doi: 10.1186/s13104-015-1283-9.

Abstract

BACKGROUND

Ipilimumab is a cytotoxic T-lymphocyte-associated protein 4 receptor antibody used for immunotherapy in cancer. Several immune-related adverse events are known. Steroid responsive encephalopathy associated with autoimmune thyroiditis is an autoimmune encephalopathy associated with Hashimoto's Disease and elevated serum levels of the related antibodies (anti-thyroid-peroxidase antibody or anti-thyroglobulin antibody). Our case implies that steroid responsive encephalopathy associated with autoimmune thyroiditis may be another previously unreported side effect of ipilimumab therapy.

CASE PRESENTATION

We report the case of a 64 years old caucasian patient with prostatic cancer who received ipilimumab therapy in a clinical trial. He presented with aphasia, tremor and ataxia, myocloni, hallucinations, anxiety and agitation in turns with somnolence. Cranial nerves, deep tendon reflexes, motor and sensory functions were normal. Electroencephalography showed background slowing but no epileptic discharges. Brain magnetic resonance imaging was normal and showed no signs of hypophysitis. Cerebrospinal fluid findings ruled out infection and neoplastic meningitis. Anti-thyroid antibodies (anti-thyroid-peroxidase antibody and anti-thyroglobulin antibody) were heavily increased. Assuming steroid responsive encephalopathy associated with autoimmune thyroiditis the patient was treated with 1,000 mg methylprednisolone i.v. for 3 days and continued with 1 mg/kg orally. On the 3rd day of treatment the patient's condition started to improve. Within the next few days he gradually returned to his previous state, and electroencephalography eventually showed only slight slowing. Seven months later the patient's condition was stable, and anti-thyroid antibodies were no more detectable.

CONCLUSION

Steroid responsive encephalopathy associated with autoimmune thyroiditis may be a hitherto unrecognized complication of ipililumab treatment and should be taken into consideration in patients developing central nervous symptoms undergoing this treatment.

摘要

背景

伊匹单抗是一种用于癌症免疫治疗的细胞毒性T淋巴细胞相关蛋白4受体抗体。已知有几种免疫相关不良事件。与自身免疫性甲状腺炎相关的类固醇反应性脑病是一种与桥本氏病以及相关抗体(抗甲状腺过氧化物酶抗体或抗甲状腺球蛋白抗体)血清水平升高相关的自身免疫性脑病。我们的病例表明,与自身免疫性甲状腺炎相关的类固醇反应性脑病可能是伊匹单抗治疗另一种先前未报告的副作用。

病例报告

我们报告了一例64岁的前列腺癌白种男性患者,其在一项临床试验中接受了伊匹单抗治疗。他依次出现失语、震颤、共济失调、肌阵挛、幻觉、焦虑和激越,并伴有嗜睡。颅神经、深腱反射、运动和感觉功能均正常。脑电图显示背景活动减慢,但无癫痫放电。脑磁共振成像正常,未显示垂体炎迹象。脑脊液检查结果排除了感染和肿瘤性脑膜炎。抗甲状腺抗体(抗甲状腺过氧化物酶抗体和抗甲状腺球蛋白抗体)大幅升高。假定为与自身免疫性甲状腺炎相关的类固醇反应性脑病,患者接受了3天静脉注射1000mg甲泼尼龙治疗,并继续口服1mg/kg。治疗第3天患者病情开始改善,并在接下来几天逐渐恢复至先前状态,脑电图最终仅显示轻微减慢。7个月后患者病情稳定,抗甲状腺抗体不再可检测到。

结论

与自身免疫性甲状腺炎相关的类固醇反应性脑病可能是伊匹单抗治疗迄今未被认识的并发症,对于接受该治疗并出现中枢神经系统症状的患者应予以考虑。

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