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本文总结73例甲状腺机能亢进性肌病(简称甲亢肌病),并作临床分析如下.临床资料一、对象1982年1月～1989年12月间我院内分泌专科门诊和住院确诊的甲亢389例中经临床、实验室、肌电图等确诊为甲亢肌病73例(男43、女30例),年龄16～69岁,平均38.2岁.病程自1个月至12年.二、各型甲亢肌病的诊断标准本组甲亢肌病包括下列3型:慢性甲亢肌病(CTM);甲亢性周期麻痹(TPP);突眼性眼肌麻痹.各型的诊断标准如下:(-)CTM临床诊断标准 1.临床确诊为甲亢;2.有明显的肌无力表现伴或不伴肌萎缩;3.
This article summarizes 73 cases of hyperthyroidism myopathy (referred to as hyperthyroidism myopathy), and for clinical analysis as follows.Clinical data A, from January 1982 to December 1989 in our hospital endocrine specialist outpatient and inpatient diagnosis of hyperthyroidism 389 cases In clinical, laboratory, electromyography and other diagnosed hyperthyroidism myopathy in 73 cases (43 males and 30 females), aged 16 to 69 years, mean 38.2 years. The course of disease from 1 month to 12 years. Second, the various types Diagnostic criteria of hyperthyroidism mycosis Myelofacial myopathy includes the following three types: chronic hyperthyroidism myopathy (CTM); hyperthyroidism periodic paralysis (TPP); ophthalmic ophthalmoplegia. Each type of diagnostic criteria are as follows: (-) CTM Clinical diagnostic criteria 1. Clinical diagnosis of hyperthyroidism; 2. There was a clear muscle weakness with or without muscle atrophy; 3.