首页> 外文期刊>Acta Neurochirurgica >Superficial siderosis of the central nervous system: secondary progression despite successful surgical treatment, mimicking amyotrophic lateral sclerosis. Case report and review
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Superficial siderosis of the central nervous system: secondary progression despite successful surgical treatment, mimicking amyotrophic lateral sclerosis. Case report and review

机译:中枢神经系统浅表铁屑病:尽管手术治疗成功,但继发性进展,模仿了肌萎缩性侧索硬化症。病例报告和审查

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摘要

Superficial siderosis of the central nervous system is a rare disorder with hemosiderin deposition in the spinal and cranial leptomeninges and subpial layer, mostly from repetitive subarachnoid hemorrhage. Progressive sensorineural deafness, cerebellar ataxia, and pyramidal signs comprise the typical clinical presentation. We describe a 47-year-old patient, who showed initial 2-year improvement after successful occlusion of an intradural bleeding source at T4. Secondary progression of symptoms without further bleedings was noted thereafter, with a clinical picture of amyotrophic lateral sclerosis. This case illustrates that the disease may progress secondarily even without re-bleedings, and that secondary progression might be due to a similar pathomechanism as in amyotrophic lateral sclerosis.
机译:中枢神经系统浅表铁皮病是一种罕见的疾病,在脊髓和颅脑软脑膜以及皮下层中有含铁血黄素沉积,主要是由于重复性蛛网膜下腔出血所致。进行性感觉神经性耳聋,小脑性共济失调和锥体束征是典型的临床表现。我们描述了一个47岁的患者,该患者在T4成功阻塞硬膜内出血源后显示出最初的2年改善。此后注意到症状继发进展而无进一步出血,并伴有肌萎缩性侧索硬化症的临床表现。该病例说明,即使没有再次出血,该疾病也可能继发发展,继发性进展可能是由于与肌萎缩性侧索硬化症相似的病理机制引起的。

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