甲巯咪唑致格雷夫斯病患者抗甲状腺关节炎综合征1例

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM
Muneo Kawasumi, Mitsunobu Kubota, Yoko Yoshii, Tadahiro Tokunaga
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引用次数: 0

摘要

摘要:本文报道抗甲状腺关节炎综合征(AAS),这是一种罕见的抗甲状腺药物的不良反应。AAS表现为严重的症状,包括肌痛、关节痛、关节炎、发烧和使用抗甲状腺药物引起的皮肤出疹。我们遇到了一名55岁的女性,在开始使用甲巯咪唑(MMI)治疗Graves病的第23天,她的手和前臂剧烈疼痛,多个关节包括膝盖、脚踝、手和手腕关节痛。血液测试显示,c反应蛋白和白细胞介素-6等炎症标志物升高,手部磁共振成像证实了炎症的发现。停用MMI后第25天,症状有改善的趋势。之后,炎症指标也下降到几乎正常的范围。除上述发现外,抗中性粒细胞细胞质抗体的缺乏和大多数血管炎症状(如肾炎、皮肤或肺部病变)可导致AAS的诊断。停药61天后,除右手第二至第四指出现轻度关节痛外,其他症状均无缓解。虽然发病机制尚不清楚,但MMI药物淋巴细胞刺激试验阳性和AAS发病前几周提示与IV型过敏反应有关。根据对Graves病的明确治疗方法的讨论,患者选择了放射性碘消融131I,并改善了甲状腺功能。我们的病例表明了对AAS的认识的重要性,这是一种罕见的、未被充分认识的、但危及生命的抗甲状腺药物的不良反应。学习要点:临床医生应该意识到在接受抗甲状腺药物治疗的患者中发生抗甲状腺关节炎综合征(AAS)的可能性,这可能导致严重的迁移性多发性关节炎。及时停用抗甲状腺药物是解决AAS的关键。抗中性粒细胞胞浆抗体(ANCA)阴性需要与抗甲状腺药物诱导的ANCA相关血管炎区分,后者表现为类似AAS的关节炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antithyroid arthritis syndrome caused by methimazole in a patient with Graves' disease.

Antithyroid arthritis syndrome caused by methimazole in a patient with Graves' disease.

Antithyroid arthritis syndrome caused by methimazole in a patient with Graves' disease.

Antithyroid arthritis syndrome caused by methimazole in a patient with Graves' disease.

Summary: This is a report on antithyroid arthritis syndrome (AAS) which is a rare adverse effect of antithyroid agents. AAS presents with severe symptoms including myalgia, arthralgia, arthritis, fever, and skin eruption due to the use of antithyroid agents. We encountered a 55-year-old woman with severe pain in the hand and forearm and arthralgia in multiple joints, including the knee, ankle, hand, and wrist on day 23 after initiation of methimazole (MMI) for Graves' disease. Blood tests revealed elevated inflammation markers such as C-reactive protein and interleukin-6, and magnetic resonance imaging of the hands confirmed inflammation findings. After withdrawing MMI on day 25, symptoms showed a tendency toward improvement. Afterwards, inflammation markers also dropped to an almost normal range. In addition to the above findings, the absence of anti-neutrophil cytoplasmic antibodies and most vasculitis symptoms such as nephritis, skin, or pulmonary lesions led to the diagnosis of AAS. A resolution of symptoms, except for mild arthralgia in the second to fourth fingers of the right hand, was observed 61 days after discontinuation of MMI. Although the pathogenesis is unclear, the positive drug lymphocyte stimulation test for MMI and the several weeks before the onset of AAS suggested involvement of a type IV allergic reaction. Based on a discussion of definitive treatment for Graves' disease, radioactive iodine ablation with 131I, which was selected by the patient, was performed and improved her thyroid function. Our case demonstrates the importance of awareness regarding AAS, which is a rare and under-recognized, but life-threatening adverse effect of antithyroid agents.

Learning points: Clinicians should be aware of the possibility of developing antithyroid arthritis syndrome (AAS) in patients treated with antithyroid medications, which can lead to severe migratory polyarthritis. Prompt cessation of the antithyroid agent is essential for the resolution of AAS. Anti-neutrophil cytoplasmic antibody (ANCA) negativity is needed to differentiate from antithyroid agent-induced ANCA-associated vasculitis, which shows arthritis similar to AAS.

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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
142
审稿时长
9 weeks
期刊介绍: Endocrinology, Diabetes & Metabolism Case Reports publishes case reports on common and rare conditions in all areas of clinical endocrinology, diabetes and metabolism. Articles should include clear learning points which readers can use to inform medical education or clinical practice. The types of cases of interest to Endocrinology, Diabetes & Metabolism Case Reports include: -Insight into disease pathogenesis or mechanism of therapy - Novel diagnostic procedure - Novel treatment - Unique/unexpected symptoms or presentations of a disease - New disease or syndrome: presentations/diagnosis/management - Unusual effects of medical treatment - Error in diagnosis/pitfalls and caveats
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