马尔尼菲青霉菌病被误诊为非典型结核性关节炎，皮肌炎或者结节性多发性动脉炎。
The case of penicilliposis marneffei was misdiagnosed as atypical tuberculous arthritis, dermatomyositis or polyarteritis nodosa.
目的探讨幼年型皮肌炎的临床特点。
Objective to investigate the clinical characteristics of juvenile dermatomyositis (JDM).
目的探讨皮肌炎的临床特点。
Objective to investigate the clinic characteristic of dermatomyositis (DM).
目的探讨皮肌炎的临床特点。
Objective the objective is to discuss the clinical features of DM.
显然青少年型皮肌炎是血管内皮细胞病。
We speculates that juvenile dermatomyositis may be a microvascular endotheliopathy.
目的：探讨运用传统中医疗法治疗皮肌炎。
Objective: to explore the use of traditional Chinese medical for treating dermatomyositis.
眼睑红斑、水肿、淡紫色是皮肌炎的特征。
Erythema, edema, and a purple (heliotrope) discoloration of the eyelids are indicative of dermatomyositis.
目的探讨皮肌炎心脏损害发生的临床特点。
目的了解皮肌炎患者呼吸中枢肺的功能变化。
Objective To investigate the changes of central respiratory drive and inspiratory muscle function in patients with dermatomyositis.
方法收集185例皮肌炎的临床资料，进行回顾性分析。
Methods Clinical information of 185 cases of dermatomyositis was collected and retrospectively analyzed.
目的探讨多发性肌炎与皮肌炎合并肾脏损害的临床特点。
Objective To investigate the clinical features of renal involvement in patients with polymyositis and dermatomyositis.
结果：误诊为不典型结核性关节炎、皮肌炎、结节性多动脉炎。
Results:The case of penicilliposis marneffei was misdiagnosed as atypical tuberculous arthritis, dermatomyositis, polyarteritis nodosa.
目的探讨青少年型皮肌炎的皮肤和骨骼肌微血管病理改变规律。
Objectives to investigate pathological features in juvenile dermatomyositis, especially microangiopathy in skin and skeletal muscles.
目的探讨多发性肌炎和皮肌炎的病理变化、发病机制、治疗效果和预后。
Objective to study the pathology, the pathogenesis, the effect of treatment and the prognosis of polymyositis and dermatomyositis.
目的：探讨多发性肌炎和皮肌炎起病不同时间的肌电图与肌酶的演变规律。
Objective:To study the difference of electromyography(EMG) and muscle enzyme(ME) in the progression of polymyositis(PM) and dermatomyositis(DM).
多发性肌炎、皮肌炎的临床表现多样化，尤其对于轻型患者鉴别诊断更加困难。
The Clinical Manifestations of polymyositis and dermatomyositis vary greatly. It is more difficult to distinguish the mild cases from others.
观察116例皮肌炎患者的肌肉病变，最常见的主诉是肌无力(81.03%)。
The muscle changes were observed in 116 patients with dermatomyositis. Muscle weakness was the most common symptom (81.03%).
近来，包涵体肌炎、皮肌炎、多发性肌炎中几种免疫细胞类型和免疫反应过程被认定。
Several immune system cell types and processes have been recently identified in muscle in inclusion body myositis dermatomyositis and polymyositis.
其中系统性红斑狼疮5例，类风湿、风湿性病变4例，进行性系统性硬化症2例，皮肌炎2例。
Among the 13 cases there were 5 cases with SLE 4 cases with rheumatoid and rheumatic disorders 2 cases with progressive systemic sclerosis and 2 cases with dermatomyositis.
治疗参照红斑狼疮、硬皮病、皮肌炎的治法，以养阴清热、凉血解毒为主，结合临床表现加味。
Treatment of reference lupus erythematosus, scleroderma, dermatomyositis governance law to Yangyin Qingre, mainly Liangxue detoxification with clinical manifestations Jiawei.
从临床表现、生化检查、肌电图及肌肉活检等方面进行分析，提出多发性肌炎与皮肌炎的诊断条件。
Analysing the data of the clinical manifestations, biochemical tests, electromyographes and muscular biopsies, the authors proposed the diagnostic criteria of polymyositis and dermatomyositis.
其他如植物神经功能失调，内分泌功能障碍，更年期综合征、甲状腺机能减退，重症肌无力，皮肌炎等。
Others such as autonomic dysfunction, endocrine dysfunction, menopause syndrome, hypothyroidism, myasthenia gravis, dermatomyositis and so on.
结果 在确诊的146例多发性肌炎和皮肌炎患者中，107例（73.29%）首诊于皮肤科，仅4例（2.74%）首诊于肾脏科；
Results Of the 146 patients confirmed with polymyositis and dermatomyositis, 107(73.29%) visited Department of Dermatology first, while only 4(2.74%) visited Department of Nephrology first.
结果 在确诊的146例多发性肌炎和皮肌炎患者中，107例（73.29%）首诊于皮肤科，仅4例（2.74%）首诊于肾脏科；
Results Of the 146 patients confirmed with polymyositis and dermatomyositis, 107(73.29%) visited Department of Dermatology first, while only 4(2.74%) visited Department of Nephrology first.
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