[Stroke, epilepsy and abdominal pain as leading symptoms in a case of mitochondrial encephalomyopathy].

H Hohage, A Raffelsiefer, K H Rahn
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引用次数: 0

Abstract

A 17-year old girl presented with recurrent seizures, strokes, fatigue, vomiting, cerebellar ataxia, dementia and hypertrichosis. Further examinations showed jerking left-sided arm reflexes, partial internal deafness and myopathy. CT and MR of the skull revealed radiolucencies within the cerebral matter of the cortex and the medulla. Laboratory tests showed increased levels of lactate and pyruvate in serum and cerebro-spinal fluid. Microscopic examination of muscular tissue showed "ragged red fibers". Electron microscopy yielded crystal inclusions in mitochondria. The symptoms represented the complete picture of the so-called MELAS/MERRF-complex, which can be easily misdiagnosed as strokes and seizures of unknown cause.

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【以中风、癫痫和腹痛为主要症状的线粒体脑肌病一例】。
一名17岁女孩,表现为反复发作、中风、疲劳、呕吐、小脑性共济失调、痴呆和多毛。进一步检查显示左臂反射抽搐,部分内聋和肌病。颅骨的CT和MR显示大脑皮层和髓质的放射性。实验室检查显示血清和脑脊液中乳酸和丙酮酸水平升高。肌肉组织镜检显示“红色纤维不规则”。电镜观察发现线粒体内有晶体包裹体。这些症状代表了所谓MELAS/ merrf复合物的全貌,它很容易被误诊为中风和不明原因的癫痫发作。
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