Jeffree Rosalind L, Wills Edward J, Harper Clive
Department of Neuropathology, University of Sydney and Royal Prince Alfred Hospital, Camperdown, NSW 2006, Australia.
Muscle Nerve. 2007 Jul;36(1):118-22. doi: 10.1002/mus.20740.
We report a 52-year-old woman who presented with a 6-month history of proximal muscle weakness, elevated serum creatine kinase, and myopathic pattern on electromyography (EMG). Histology of the muscle shows a speckled pattern due to clustering of enlarged mitochondria. The pathology resembles that of selenium deficiency. The patient was found to have borderline low serum selenium and also low vitamin D and thyroid-stimulating hormone. The cause of this unusual myopathy is probably multifactorial. This case is important because the unusual pathological picture represents a potentially treatable myopathy. In addition, we hope that publication of the complex clinical and biochemical abnormalities of this case, in conjunction with other case reports, may facilitate future elucidation of muscle mitochondrial function and dysfunction.
我们报告了一名52岁女性,她有6个月的近端肌无力病史,血清肌酸激酶升高,肌电图(EMG)显示肌病模式。肌肉组织学检查显示,由于线粒体增大聚集,呈现斑点状模式。病理表现类似于硒缺乏症。该患者血清硒水平临界偏低,维生素D和促甲状腺激素水平也较低。这种不寻常的肌病病因可能是多因素的。该病例很重要,因为这种不寻常的病理表现代表了一种潜在可治疗的肌病。此外,我们希望通过发表该病例复杂的临床和生化异常情况,并结合其他病例报告,可能有助于未来阐明肌肉线粒体的功能和功能障碍。