肉瘤样恶性胸膜间皮瘤伴抗ma2相关副肿瘤神经综合征1例报告

IF 0.2 Q4 ONCOLOGY
Akio Tada , Kozo Kuribayashi , Kazuhiro Kitajima , Akifumi Nakamura , Michiko Yuki , Shingo Kanemura , Eisuke Shibata , Yoshiki Negi , Hirotoshi Ishigaki , Yasuhiro Nakajima , Ryo Takahashi , Takashi Yokoi , Toshiyuki Minami , Takashi Kijima
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引用次数: 0

摘要

副肿瘤神经系统综合征(PNS)很少与恶性胸膜间皮瘤(MPM)相关。我们报告了2018年1月诊断为小脑变性的63岁女性的第一例肉瘤样间皮瘤。全身检查显示右侧胸膜增厚。肿块的胸膜活检显示肉瘤样MPM cT3N0M0。2018年2月,抗ma2抗体阳性提示PNS合并MPM。首先给予顺铂(75 mg/m2) +培美曲塞(500 mg/m2)化疗。对于PNS,给予类固醇脉冲治疗和大剂量免疫球蛋白治疗。MPM可能引起抗ma2抗体相关的PNS。早期诊断和开始抗癌治疗和免疫治疗是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sarcomatoid malignant pleural mesothelioma associated with anti-Ma2-related paraneoplastic neurological syndrome: A case report

Paraneoplastic neurological syndrome (PNS) is rarely associated with malignant pleural mesothelioma (MPM). We report the first case of sarcomatoid mesothelioma in a 63-year-old female diagnosed with cerebellar degeneration in January 2018. Systemic examination showed right pleura thickening. The pleural biopsy of the mass revealed a sarcomatoid MPM cT3N0M0. In February 2018, anti-Ma2 antibody positivity indicated PNS complicated with MPM. First, cisplatin (75 mg/m2) + pemetrexed (500 mg/m2) chemotherapy was given. For PNS, steroid pulse therapy and high-dose immunoglobulin therapy were administered. MPM may cause anti-Ma2 antibody-related PNS. Early diagnosis and starting anticancer treatment and immunotherapy are critical.

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