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阿诺德-奇亚里畸形中的急性呼吸衰竭与睡眠呼吸障碍

Acute respiratory failure and sleep-disordered breathing in Arnold-Chiari malformation.

作者信息

Tsara Venetia, Serasli Eva, Kimiskidis Vassilios, Papagianopoulos Sotirios, Katsaridis Vassilios, Fylaktakis Makedos, Christaki Pandora, Kazis Aristidis

机构信息

Second Chest Department of Aristotle University, School of Medicine, George Papanikolaou Hospital, Thessaloniki, Greece.

出版信息

Clin Neurol Neurosurg. 2005 Oct;107(6):521-4. doi: 10.1016/j.clineuro.2004.10.008.

Abstract

We report on the case of a 32-year-old man who was admitted after an episode of acute respiratory failure. Clinical and laboratory investigations revealed nocturnal hypoventilation with predominately obstructive sleep apneas accompanied by lower cranial nerve palsies, cerebellar and mild pyramidal signs. Magnetic resonance imaging disclosed Arnold-Chiari type I malformation with syringomyelia. Transcranial magnetic stimulation demonstrated the integrity of the corticodiaphragmatic pathway and it was postulated that the respiratory disorder was mainly due to the severe and irreversible lower cranial nerve palsies. Two years after decompressive craniectomy, sleep disordered-breathing persisted despite no radiological evidence of brain stem compression. Nevertheless, non-invasive positive pressure ventilation (NIPPV) during sleep proved to be quite effective in the management of the patient's refractory respiratory insufficiency. In conclusion, Arnold-Chiari type I may rarely present with acute respiratory failure and sleep apneas. An electrophysiological investigation into the mechanism of the respiratory dysfunction is presented.

摘要

我们报告了一例32岁男性患者,该患者在一次急性呼吸衰竭发作后入院。临床和实验室检查显示夜间通气不足,主要为阻塞性睡眠呼吸暂停,并伴有低位颅神经麻痹、小脑体征和轻度锥体束征。磁共振成像显示I型阿诺德-基亚里畸形伴脊髓空洞症。经颅磁刺激显示皮质-膈肌通路完整,推测呼吸障碍主要是由于严重且不可逆的低位颅神经麻痹所致。减压颅骨切除术后两年,尽管没有脑干受压的影像学证据,但睡眠呼吸障碍仍然存在。然而,睡眠期间的无创正压通气(NIPPV)被证明对治疗该患者难治性呼吸功能不全非常有效。总之,I型阿诺德-基亚里畸形可能很少表现为急性呼吸衰竭和睡眠呼吸暂停。本文对呼吸功能障碍的机制进行了电生理研究。

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