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1例甲状腺毒症性肌病伴全身肌肉萎缩(包括舌肌),无突眼性甲状腺肿的体征表现

[A case of thyrotoxic myopathy with generalized body muscular atrophy including the tongue muscle, lacking physical manifestations of Basedow disease].

作者信息

Kitahara Sho, Tonouchi Takahumi, Otsu Yutaka, Kawachi Izumi, Oyake Mutsuo, Fujita Nobuya

机构信息

Department of Neurology, Nagaoka Red Cross Hospital.

Department of Neurology, Niigata University Medical and Dental Hospital.

出版信息

Rinsho Shinkeigaku. 2020 Oct 24;60(10):677-681. doi: 10.5692/clinicalneurol.cn-001365. Epub 2020 Sep 5.

Abstract

We report a 74-year-old man with a 2-year history of proximal limb pain, body weight loss of 15 kg, and muscle weakness. Muscle atrophy was evident in the limbs and trunk, as well as the tongue. He was admitted to our hospital with suspected amyotrophic lateral sclerosis (ALS). Although he had no physical manifestations of Basedow disease such as palpitations, hyperhidrosis, hand tremor, exophthalmos, and an enlarged thyroid, he was diagnosed as having thyrotoxic myopathy as laboratory examinations indicated hyperthyroidism and positivity for TSH receptor antibody. The serum level of soluble IL-2 receptor was also elevated. Despite the severe muscle atrophy, the serum CK level was normal. A biopsy from the left quadriceps muscle revealed Type 1 fibers atrophy. Administration of anti-thyroid drugs normalized his thyroid function and the level of soluble IL-2 receptor, leading to improvement of the generalized muscle atrophy.

摘要

我们报告了一名74岁男性,有近端肢体疼痛病史2年,体重减轻15千克,伴有肌肉无力。四肢、躯干以及舌头均明显出现肌肉萎缩。他因疑似肌萎缩侧索硬化症(ALS)入院。尽管他没有如心悸、多汗、手部震颤、突眼和甲状腺肿大等巴塞多氏病的体征,但实验室检查显示甲状腺功能亢进且促甲状腺激素受体抗体呈阳性,因此被诊断为甲状腺毒症性肌病。血清可溶性白细胞介素-2受体水平也升高。尽管存在严重的肌肉萎缩,但血清肌酸激酶水平正常。左股四头肌活检显示1型纤维萎缩。使用抗甲状腺药物使他的甲状腺功能和可溶性白细胞介素-2受体水平恢复正常,全身肌肉萎缩情况得到改善。

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