Eosinofiele fasciitis na immuuncheckpointinhibitie met pembrolizumab

J. Vanhees, F. Lockefeer, C. Bohyn, E. Vandenbroucke, M. Lebeer
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引用次数: 1

Abstract

Eosinophilic fasciitis following checkpoint inhibitor therapy with pembrolizumab A 70-year-old woman presents with progressive induration of the skin and oedema spreading to the 4 limbs. She has been treated for 8 months with pembrolizumab for a stage IVa non-small-cell adenocarcinoma of the right lung. A blood test reveals eosinophilia. The MRI of the left forearm shows oedematous thickening of the superficial and deep intermuscular fascia, consistent with fasciitis. On the biopsy, fascial thickening and accumulation of lymphocytes is observed. The diagnosis of eosinophilic fasciitis is made, presumably triggered by pembrolizumab. After multidisciplinary consultation at the Belgian Multidisciplinary Immunotoxicity Board (BITOX), the treatment with pembrolizumab is discontinued. The patient is administered methylprednisolone 1 mg/kg and achieves complete remission of the symptoms.
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使用pembrolizumab的免疫检查点抑制剂引发卵磷脂性筋膜炎
pembrolizumab检查点抑制剂治疗后嗜酸性筋膜炎一名70岁女性表现为进行性皮肤硬化和四肢水肿扩散。她因右肺IVa期非小细胞腺癌接受了8个月的派姆单抗治疗。血液检查显示嗜酸性粒细胞增多。左前臂MRI显示肌间浅筋膜和深筋膜水肿增厚,符合筋膜炎。活检显示筋膜增厚,淋巴细胞聚集。诊断为嗜酸性筋膜炎,可能由派姆单抗触发。在比利时多学科免疫毒性委员会(BITOX)的多学科咨询后,停止使用派姆单抗治疗。患者给予甲基强的松龙1mg /kg,症状完全缓解。
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