抗程序细胞死亡蛋白1抗体治疗期间亚急性甲状腺炎1例报告

Makiko Ikemoto , Yasufumi Seki , Daisuke Watanabe , Toshio Takagi , Atsuhiro Ichihara
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引用次数: 0

摘要

免疫检查点抑制剂(ICI)治疗偶尔会诱发甲状腺毒症,作为ICI相关的不良反应。在ICI治疗期间甲状腺毒症的病因是无痛性甲状腺炎,在大多数情况下被归类为破坏性甲状腺炎。然而,另一种形式的破坏性甲状腺炎,亚急性甲状腺炎,很少被报道。在这里,我们报告了一例亚急性甲状腺炎,在抗程序性细胞死亡蛋白1 (PD-1)抗体派姆单抗治疗期间出现。病例介绍:一名45岁男性因肾细胞癌行半肾切除术后接受派姆单抗治疗。在第6次给药后2周,即首次给药27周后,患者抱怨颈部疼痛,同时血清c反应蛋白和甲状腺激素水平升高,尽管没有感染症状。甲状腺超声检查发现低回声病变,99m甲状腺显像显示甲状腺摄取减少,诊断为亚急性甲状腺炎。最大剂量20 mg强的松龙治疗4周后,甲状腺激素水平恢复正常,在随后的三个疗程的派姆单抗治疗中,甲状腺激素水平保持在正常范围内。结论:我们报告了一例在派姆单抗治疗期间发生亚急性甲状腺炎的病例,强调了在ICI治疗期间调查甲状腺毒症病因的重要性,并提出了ICI治疗与亚急性甲状腺炎发展之间的潜在关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subacute thyroiditis during anti-programmed cell death protein 1 antibody therapy: A case report

Introduction

Immune checkpoint inhibitor (ICI) therapies can occasionally induce thyrotoxicosis as an ICI-associated adverse effect. The etiology of thyrotoxicosis during ICI therapy is painless thyroiditis, which is classified as destructive thyroiditis, in most cases. However, another form of destructive thyroiditis, subacute thyroiditis, has rarely been reported. Here, we present a case of subacute thyroiditis that emerged during anti-programmed cell death protein 1 (PD-1) antibody pembrolizumab therapy.

Case presentation

A 45-year-old man underwent pembrolizumab therapy after undergoing heminephrectomy for renal cell carcinoma. Two weeks after the 6th dose of pembrolizumab, administered 27 weeks following the initial administration, the patient complained of neck pain alongside increased levels of serum C-reactive protein and thyroid hormones, despite the absence of infectious symptoms. Upon thyroid echography, a hypoechoic lesion was observed, and technetium-99m thyroid scintigraphy revealed reduced thyroid uptake, the patient was diagnosed with subacute thyroiditis. Treatment with a maximum dose of 20 mg of prednisolone for 4 weeks normalized thyroid hormone levels, which remained within the normal range throughout the subsequent three courses of pembrolizumab therapy.

Conclusion

We present a case of subacute thyroiditis during pembrolizumab therapy, highlighting the importance of investigating the etiology of thyrotoxicosis during ICI therapy and proposing a potential association between ICI therapy and the development of subacute thyroiditis.
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