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[急性呼吸衰竭作为阿诺德-奇亚里畸形的首发症状。两例报告]

[Acute respiratory failure as the sol inaugural sign of Arnold-Chiari malformation. Two cases].

作者信息

Chaouch N, Meraï S, Cheikh Rouhou S, Ben Romdhane K, Ben Mrad S, Besbes M, Tritar F

机构信息

Service de Pneumologie, Pavillon C, Hôpital de Pneumo-Phtisiologie Abderrahman-Mami, 2080 L'Ariana/Tunis, Tunisia.

出版信息

Rev Pneumol Clin. 2007 Oct;63(5 Pt 1):319-22. doi: 10.1016/s0761-8417(07)74209-8.

Abstract

Arnold-Chiari malformation is an occipitocervical malformation where the cerebellar amygdales descend below the occipital foramen. Acute respiratory failure is an exceptional inaugural sign. We report two cases disclosed by alveolar hypoventilation associated with type I Arnold-Chiari malformation. The two patients age 51 and 52 years had an uneventful past history and presented with hypercapnic encephalopathy with acute respiratory failure requiring ventilatory assistance. Respiratory function tests, helicoidal thoracic computed tomographic angiography, electromyogram, cardiac echography, and thyroid and immunological tests were normal. Blood gases and polysomnography were in favor of central hypoventilation without sleep apnea. Magnetic resonance imaging demonstrated type I Arnold-Chiari malformation. The course was complicated by recurrent respiratory failure in both patients. Surgical decompression performed for the first patient provided no improvement. This patient died two months after surgery subsequent to aspiration pneumonia. The second patient was treated with continuous positive pressure noninvasive ventilatory assistance and had a good outcome at 25 months. These two cases illustrate the absence of any neurological sign, acute respiratory failure being the only sign of Arnold-Chiari malformation.

摘要

阿诺德-奇亚里畸形是一种枕颈畸形,小脑扁桃体降至枕骨大孔以下。急性呼吸衰竭是一种罕见的首发症状。我们报告两例与I型阿诺德-奇亚里畸形相关的肺泡通气不足所致的病例。两名患者年龄分别为51岁和52岁,既往史无异常,均表现为高碳酸血症性脑病伴急性呼吸衰竭,需要通气支持。呼吸功能测试、螺旋胸部计算机断层血管造影、肌电图、心脏超声以及甲状腺和免疫学检查均正常。血气分析和多导睡眠图显示为中枢性通气不足,无睡眠呼吸暂停。磁共振成像显示为I型阿诺德-奇亚里畸形。两名患者的病程均因反复呼吸衰竭而复杂化。为第一名患者进行的手术减压未取得改善。该患者在术后两个月因吸入性肺炎死亡。第二名患者接受持续气道正压无创通气支持治疗,25个月时预后良好。这两例病例表明不存在任何神经学体征,急性呼吸衰竭是阿诺德-奇亚里畸形的唯一体征。

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