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A Rare Case of Ipilimumab-induced Reversible Hypophysitis and Permanent Primary Hypothyroidism

机译:罕见的伊立木单抗诱发的可逆性垂体炎和永久性原发性甲状腺功能减退症

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Ipilimumab is a monoclonal antibody targeting the cytotoxic T-lymphocyte antigen-4 receptor, which was originally approved for the treatment of metastatic melanoma. It is the first immune checkpoint inhibitor to enter clinical practice. Immune toxicity due to ipilimumab causing colitis, hepatitis, and dermatitis are well-described in literature. We report a case of hypophysitis?resolving with corticosteroid treatment, following which?the patient developed long-term primary thyroid impairment. This highlights the importance of vigilance for rarer immune-related toxicities as clinical utilization of ipilimumab becomes more widespread.
机译:伊匹木单抗是靶向细胞毒性T淋巴细胞抗原4受体的单克隆抗体,最初被批准用于治疗转移性黑色素瘤。它是第一个进入临床实践的免疫检查点抑制剂。依匹莫单抗引起的结肠炎,肝炎和皮炎引起的免疫毒性在文献中已有很好的描述。我们报告一例垂体炎,用皮质类固醇激素治疗,此后患者发展为长期原发性甲状腺功能减退。随着伊立木单抗的临床应用变得更加广泛,这突出了对罕见的免疫相关毒性保持警惕的重要性。

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