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Leigh综合征

Leigh's syndrome.

作者信息

Mannan A A S R, Sharma M C, Shrivastava P, Ralte A M, Gupta V, Behari M, Sarkar C

机构信息

Department of Pathology, All India Institute of Medical Sciences, New Delhi 110-029, India.

出版信息

Indian J Pediatr. 2004 Nov;71(11):1029-33. doi: 10.1007/BF02828121.

Abstract

A 15-month-old female child presented with sudden onset cough and hyperventilation along with evidence of metabolic acidosis. She had past history of recurrent vomiting, episodes of abnormal posturing, difficulty in deglutition and regression of milestones since 12 months of age. CT scan of the brain revealed hypodense lesions in bilateral basal ganglia and on MRI there were T2 hyperintensities in bilateral lentiform nuclei, caudate nuclei, thalamus, red nuclei and dentate nuclei. Biochemical examination revealed persistently elevated serum lactate levels with high lactate/pyruvate ratio. Resuscitative measures were of no avail and the child succumbed to the illness on the second day of admission. Neuropathological examination at autopsy demonstrated marked spongiosis, focal necrosis, endothelial proliferation, reactive astrogliosis and extensive demyelination involving bilateral basal ganglia, midbrain and spinal cord which were typical of Leigh's sub acute necrotizing encephalomyelopathy.

摘要

一名15个月大的女童出现突发咳嗽、呼吸急促以及代谢性酸中毒迹象。她有反复呕吐、异常姿势发作、吞咽困难和自12个月大起发育里程碑倒退的既往史。脑部CT扫描显示双侧基底神经节低密度病变,MRI显示双侧豆状核、尾状核、丘脑、红核和齿状核T2高信号。生化检查显示血清乳酸水平持续升高,乳酸/丙酮酸比值升高。复苏措施无效,患儿在入院第二天死亡。尸检时的神经病理学检查显示双侧基底神经节、中脑和脊髓有明显的海绵样变、局灶性坏死、内皮细胞增生、反应性星形胶质细胞增生和广泛脱髓鞘,这是Leigh亚急性坏死性脑脊髓病的典型表现。

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