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Pembrolizumab-induced agranulocytosis in a pulmonary pleomorphic carcinoma patient who developed interstitial lung disease and ocular myasthenia gravis

机译:帕姆单抗诱导的粒细胞增多症在肺多形性肺癌患者中发生间质性肺疾病和重症肌无力

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An 82-year-old man with a recurrence of pulmonary pleomorphic carcinoma was treated with pembrolizumab. He achieved partial response after three cycles of pembrolizumab. However, he developed febrile neutropenia. A bone marrow aspiration sample revealed a decrease of mature neutrophils, and anti-neutrophil antibody was detected in blood. Computed tomography scans revealed consolidation in the right lung. Pathological findings in lung biopsy tissue revealed organizing pneumonia. Pembrolizumab-induced agranulocytosis and interstitial lung disease (ILD) were diagnosed. We initiated antibacterial therapy and granulocyte colony-stimulating factor (G-CSF). The neutrophil count immediately increased, and the fever decreased. The improvement of ILD was achieved without using systemic steroids. Moreover, the patient developed ocular myasthenia gravis induced by pembrolizumab. This is the first case report of pembrolizumab-induced agranulocytosis. Agranulocytosis was improved by administration of G-CSF without using systemic steroids. However, further studies are needed to determine the optimal treatment for patients with anti-neutrophil antibody whose tumor has progressed.
机译:接受pembrolizumab治疗的82岁肺部多形性癌复发男子。经过三轮pembrolizumab治疗后,他获得了部分缓解。但是,他出现了发热性中性粒细胞减少症。骨髓抽吸样品显示成熟的中性粒细胞减少,血液中检测到抗中性粒细胞抗体。计算机体层摄影术扫描显示右肺巩固。肺活检组织中的病理发现显示有组织性肺炎。诊断为Pembrolizumab诱导的粒细胞缺乏症和间质性肺疾病(ILD)。我们启动了抗菌治疗和粒细胞集落刺激因子(G-CSF)。中性粒细胞计数立即增加,发烧减少。 ILD的改善无需使用全身性类固醇。此外,患者发生了由派姆单抗引起的重症眼肌无力。这是派姆单抗诱导的粒细胞缺乏症的首例病例报告。不使用全身性类固醇,给予G-CSF可改善粒细胞缺乏症。但是,需要进一步的研究来确定肿瘤进展的抗中性粒细胞抗体患者的最佳治疗方法。

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