论文部分内容阅读
线粒体肌病(Mitochondrial myopathy)是一组临床表现不一、发病学上异源性疾病,除骨骼肌外可以累及多个系统(线粒体脑肌病或细胞病),通常根据骨骼肌细胞线粒体的超微结构或生物化学上的异常而确诊。我们在电镜常规诊断中发现1例,报告如下。一、临床资料患者,女,30岁。反复发作性发热,皮疹,肌肉酸疼6个月。体检:T38℃,颅神经(一),四肢肌肉压痛(+),近端肌力5度。无肌萎缩,皮疹已消退(发作时皮疹为散在性、大小不一的风团样皮损)。病理反射(一)。肌电图:所测肌肉为肌源性损害。
Mitochondrial myopathy is a group of clinically heterogeneous, morbidly heterogeneous diseases that can involve multiple systems (mitochondrial encephalomyopathy or cytopathology) in addition to skeletal muscle, usually based on the presence of mitochondrial supernumerary Microstructural or biochemical abnormalities were diagnosed. We found in the routine diagnosis of electron microscopy in 1 case, the report is as follows. First, the clinical data patients, female, 30 years old. Repeated episodes of fever, rash, muscle aches for 6 months. Physical examination: T38 ℃, cranial nerve (a), tenderness of limbs muscle (+), proximal muscle strength of 5 degrees. No muscle atrophy, rash has subsided (episodes of rash scattered, the size of the wind-like skin lesions). Pathological reflex (a). EMG: Muscle measured myogenic damage.