自身免疫性边缘脑炎合并非小细胞肺癌轻脑膜转移:对奥希替尼、免疫球蛋白、利妥昔单抗和托珠单抗的治疗反应

Seolah Lee, Seon-Jae Ahn, Han Sang Lee, Kon Chu
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引用次数: 0

摘要

当脑病患者有器质性脑损伤时,他的症状很容易而且经常被错误地归因于该脑损伤。然而,不同条件的组合也是可能的。我们报告一例自身免疫性边缘脑炎合并脑膜轻脑癌。一名57岁女性患者转至我院,有1个月的癫痫发作史和攻击行为。亚急性起病伴多局灶T2高信号病变提示自身免疫性脑炎,开始大剂量类固醇脉冲及免疫球蛋白治疗。然而,脑脊液检查显示非小细胞肺癌转移性腺癌,她处于完全缓解状态。Osimertinib是第三代表皮生长因子受体酪氨酸激酶抑制剂,在维持利妥昔单抗和托珠单抗免疫治疗的同时,开始针对瘦脑膜转移。她的神经系统症状对免疫治疗的反应有所改善,持续了大约1个月,然后再次恶化。我们的结论是,她的症状更可能是自身免疫性脑炎,而不是脑膜癌,因此停用了奥西替尼。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Autoimmune limbic encephalitis combined with leptomeningeal metastases of non-small cell lung cancer: treatment response to osimertinib, immunoglobulin, rituximab, and tocilizumab.

Autoimmune limbic encephalitis combined with leptomeningeal metastases of non-small cell lung cancer: treatment response to osimertinib, immunoglobulin, rituximab, and tocilizumab.

Autoimmune limbic encephalitis combined with leptomeningeal metastases of non-small cell lung cancer: treatment response to osimertinib, immunoglobulin, rituximab, and tocilizumab.

When a patient with encephalopathy has an organic brain lesion, his symptom is easily and often mistakenly attributed to that brain lesion. However, a combination of different conditions is also possible. We present a case of autoimmune limbic encephalitis combined with leptomeningeal carcinomatosis. A 57-year-old female patient was transferred to our institute with a 1-month history of seizure and aggressive behavior. Subacute onset of psychosis with multifocal T2 high signal lesions suggested autoimmune encephalitis, and high-dose steroid pulse and immunoglobulin therapy were started. However, a cerebrospinal fluid study revealed metastatic adenocarcinoma of non-small cell lung cancer, of which she was in complete remission state. Osimertinib, a third-generation epidermal growth factor receptor tyrosine kinase inhibitor, was started targeting leptomeningeal metastases while maintaining immunotherapy of rituximab and tocilizumab. Her neurological symptoms showed improvement in response to immunotherapy which lasted approximately 1 month and then deteriorated again. We concluded that her symptoms were more attributable to autoimmune encephalitis than leptomeningeal carcinomatosis, and discontinued osimertinib.

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