Nicoll J A, Moss T H, Love S, Campbell M J, Schutt W H
Department of Neuropathology, Frenchay Hospital, Bristol, UK.
Clin Neuropathol. 1993 Jan-Feb;12(1):38-43.
We report the clinical and autopsy findings of two patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). The cases were unusual in that both patients presented with stroke-like episodes and neither patient had clinically evident myopathy, consequently in neither case was the correct diagnosis made during life. Despite the absence of myopathy clinically, at autopsy skeletal muscle showed the characteristic features of mitochondrial cytopathy. One of the patients, in addition to the features of MELAS, also had gastrointestinal involvement at presentation which was sufficiently severe to warrant surgery and a peripheral neuropathy.
我们报告了两例患有线粒体肌病、脑病、乳酸性酸中毒和卒中样发作(MELAS)患者的临床及尸检结果。这两例病例不同寻常之处在于,两名患者均表现为卒中样发作,且均无临床明显的肌病症状,因此在生前均未做出正确诊断。尽管临床上没有肌病表现,但尸检时骨骼肌显示出线粒体细胞病的特征性表现。其中一名患者,除了具有MELAS的特征外,在发病时还伴有严重到需要手术治疗的胃肠道病变以及周围神经病变。