利妥昔单抗治疗树突细胞肉瘤并发重症肌无力1例临床报告

来源 :中国免疫学会第九届全国免疫学学术大会 | 被引量 : 0次 | 上传用户:zhangzujin
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重症肌无力是一种抗体介导的自身免疫性疾病,主要累及神经肌肉接头处的突触后膜.重症肌无力的主要临床特征是症状的波动性,其患者可并发胸腺瘤,而树突细胞肉瘤并发重症肌无力的病例罕有报道.有研究报道认为利妥昔单抗对于重症肌无力,尤其是难治性重症肌无力的患者是有效的.我们报道了一名60岁女性患者,主因波动性的肢体无力、双眼睑下垂及复视数月,吞咽及呼吸困难20天就诊,肌注新斯的明后临床症状明显改善.既往明确诊断为树突细胞肉瘤,并接受4次颈部"淋巴结切除术".
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