Ken‐ichi Shibata, T. Mukai, H. Nakagaki, S. Nagano
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引用次数: 0
摘要
对于线粒体肌病、脑病、乳酸性酸中毒和脑卒中样发作(MELAS)患者的磁共振成像结果知之甚少b> G突变。一例31岁男性患者,以头痛和左侧同质性偏盲为主诉。脑磁共振成像显示右侧枕叶弥散和T2加权成像呈高信号。诊断为MELAS,病因突变为m.3271 T > C。虽然他的症状逐渐消退,但磁共振成像显示左侧枕叶弥散性小皮质病变。我们报告一例罕见的非典型脑卒中样病变的患者与m.3271 T b> C突变的MELAS。
Disseminated small cortical lesions of stroke‐like episodes in a patient with MELAS with an m.3271 T > C mutation
Little is known about magnetic resonance imaging findings in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS) with the m.3271 A > G mutation. A 31‐year‐old man presented with headache and left‐sided homonymous hemianopsia. Brain magnetic resonance imaging showed hyperintensities in the right occipital lobe on diffusion‐ and T2‐weighted imaging. MELAS was diagnosed, and the etiological mutation was identified as m.3271 T > C. Although his symptoms gradually resolved, magnetic resonance imaging revealed disseminated small cortical lesions in the left occipital lobe. We report a rare case of atypical stroke‐like lesions in a patient with MELAS with the m.3271 T > C mutation.