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Effectiveness of long term administration of humanized anti-interleukin-6 receptor antibody (tocilizumab) for multicentric Castleman's disease with pulmonary involvement

机译:长期施用人源化抗白介素6受体抗体(tocilizumab)对多中心性Castleman病伴肺部感染的有效性

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A 27-year-old man was admitted to our hospital with the complaint of general fatigue. He had cervical and mediastinal lymphadenopathy. Laboratory examination revealed anemia, hypergammaglobulinemia, and increased levels of C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR). A chest radiograph showed opacities in both lung fields. Pathological findings from thoracoscopic mediastinal lymph node and lung biopsies were compatible with multicentric Castleman's disease (MCD), plasma cell type with pulmonary involvement. Chemotherapy combined with radiation therapy resulted in no improvement of his lymphadenopathy and inflammatory symptoms. Eight mg/kg humanized anti-human IL-6 receptor antibody (tocilitumab) was thus administered biweekly. Soon after initiating the tocilitumab treatment, the patient's general fatigue disappeared, and anemia, CRP, ESR, hypergammaglobulinemia and lymphadenopathy all improved remarkably. Further treatment with tocilitumab for two years resulted in maintenance of this good response without any severe adverse events, but the pulmonary findings showed no obvious improvement. Tocilitumab therapy was effective in this MCD patient, however its influence on concurrent lung disease needs to be investigated further.
机译:一名27岁的男子因全身疲倦而入院。他患有颈部和纵隔淋巴结肿大。实验室检查发现有贫血,高球蛋白血症,C反应蛋白(CRP)和红细胞沉降率(ESR)升高。胸部X光片显示两个肺野均混浊。胸腔镜纵隔淋巴结和肺活检的病理结果与多中心Castleman病(MCD),浆细胞类型伴有肺部侵袭相吻合。化学疗法与放射疗法的结合不会改善他的淋巴结肿大和炎症症状。因此每两周施用八mg / kg的人源化抗人IL-6受体抗体(tocilitumab)。开始使用Tocilitumab治疗后不久,患者的全身疲劳消失,贫血,CRP,ESR,高球蛋白血症和淋巴结肿大均得到明显改善。继续用托珠单抗治疗两年可维持这种良好反应,而没有任何严重的不良事件,但肺部检查结果未见明显改善。 Tocilitumab治疗对这名MCD患者有效,但是其对并发肺部疾病的影响尚需进一步研究。

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