首页> 美国卫生研究院文献>Endocrinology and Metabolism >A Rare Manifestation of Hypothyroid Myopathy: Hoffmanns Syndrome
【2h】

A Rare Manifestation of Hypothyroid Myopathy: Hoffmanns Syndrome

机译:甲状腺功能减退肌病的罕见表现:霍夫曼综合症

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Hypothyroid myopathy is observed frequently and the resolution of the clinical manifestations of myopathy following thyroid hormone replacement is well known. However, a specific subtype of hypothyroid myopathy, Hoffmann's syndrome, characterized by increased muscular mass (pseudohypertrophy), proximal muscle weakness, muscle stiffness and cramps, is rarely reported. Herein, we describe a 34-year-old male who presented with proximal muscle weakness and non-pitting edema of the lower extremities. He initially visited the neurology department where he was suspected of having polymyositis. Additional laboratory evaluation revealed profound autoimmune hypothyroidism and elevated muscle enzymes including creatine kinase. The patient was started on levothyroxine treatment and, subsequently, clinical symptoms and biochemical parameters resolved with the treatment. The present case highlights that hypothyroidism should be considered in the differential diagnosis of musculoskeletal symptoms even in the absence of overt manifestations of hypothyroidism. To our knowledge, this is the first case reported in Korea.
机译:甲状腺功能减退性肌病经常被观察到,甲状腺激素替代后肌病的临床表现的解决是众所周知的。然而,很少有甲状腺功能减退性肌病的特定亚型霍夫曼综合征,其特征是肌肉质量增加(假性肥大),近端肌肉无力,肌肉僵硬和抽筋。本文中,我们描述了一位34岁的男性患者,该患者患有下肢近端肌肉无力和无麻点性水肿。最初,他去了神经科,被怀疑患有多发性肌炎。进一步的实验室评估发现,自身免疫性甲状腺功能低下症严重,包括肌酸激酶在内的肌肉酶升高。患者开始接受左甲状腺素治疗,随后临床症状和生化参数随治疗而缓解。本病例强调,即使没有明显的甲状腺功能减退症状,在鉴别肌肉骨骼症状时也应考虑甲状腺功能减退。据我们所知,这是韩国报道的第一例。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号