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[以中枢型睡眠呼吸暂停综合征为表现的皮质小脑萎缩]

[Cortical cerebellar atrophy presenting with central type sleep apnea syndrome].

作者信息

Qingyu Jin, Nomura Takuo, Ochi Hirofumi, Taniwaki Takayuki, Furuya Hirokazu, Kira Jun-ichi

机构信息

Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University.

出版信息

Rinsho Shinkeigaku. 2005 Jul;45(7):490-4.

Abstract

The patient was a 55-year-old man who had shown progressive dysarthria and unsteady gait since 48 years of age. Neurologically, pure cerebellar ataxia without either pyramidal or extrapyramidal signs was seen. He had been diagnosed as having cortical cerebellar atrophy (CCA) at age 53. Polysomnography was carried out at June 17th, 2003, because of snoring and sleep apnea had occurred since January 2003. The results showed central dominant sleep apnea with an apnea index (AI) of 16.6. Apnea occurred during shallow sleep, stages I and II, while the length of REM sleep was almost normal, occupying 17.7% of total sleep time. The rhythm of his sleep was well preserved. Brain MRI showed cerebellar atrophy without any brainstem abnormality. Except for the central type sleep apnea, no other autonomic symptoms were found. We considered that the diagnosis of CCA remained applicable to the patient because of the presence of pure cerebellar symptoms over a 7-year-course, and the absence of brainstem atrophy on MRI. Sleep apnea seen in the present patient was distinct from MSA in which central type sleep apnea dominated, and that the sleeping rhythm including REM was preserved.

摘要

该患者为一名55岁男性,自48岁起出现进行性构音障碍和步态不稳。神经系统检查发现为单纯小脑性共济失调,无锥体束或锥体外系体征。他在53岁时被诊断为皮质小脑萎缩(CCA)。由于自2003年1月以来出现打鼾和睡眠呼吸暂停,于2003年6月17日进行了多导睡眠图检查。结果显示为中枢性为主的睡眠呼吸暂停,呼吸暂停指数(AI)为16.6。呼吸暂停发生在浅睡眠的I期和II期,而快速眼动睡眠的时长基本正常,占总睡眠时间的17.7%。其睡眠节律保存良好。脑部MRI显示小脑萎缩,无任何脑干异常。除中枢性睡眠呼吸暂停外,未发现其他自主神经症状。鉴于患者在7年病程中存在单纯小脑症状且MRI上无脑干萎缩,我们认为CCA的诊断仍然适用于该患者。本患者所见的睡眠呼吸暂停与以中枢性睡眠呼吸暂停为主的多系统萎缩不同,且包括快速眼动睡眠在内的睡眠节律得以保存。

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