Difficult Airway and Failed Tracheal Intubation in a Patient with Mucopolaysaccharidoses Type II: A Case Report

A. Cho, B. Koo, Y. Chung, Misoon Lee, Jaewoong Jung, Eun Young Ko, Seri Park, Jihun Yu
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Abstract

Mucopolysaccharidoses are rare lysosomal storage diseases resulting from defects in lysosomal enzymes involved in degradation of glycosaminoglycans. Different mucopolysaccharidoses are caused by different enzyme deficiencies The anesthetic complications are related to the organs involved. Patients with mucopolysaccharidoses are rare, and few anesthetists encounter such patients. We experienced a case of mucopolysaccharidoses type II. Several endotracheal intubation attempts were tried, but we experienced failed endotracheal intubation. And we decided to proceed with surgery under bag-mask ventilation because of the short operation time. There’s no desaturation time. And the patient’s spontaneous ventilation was recovered and awakened. We have also briefly discussed the pathophysiology, clinical features, and possible airway management options for patients with mucopolysaccharidoses type II.
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II型粘多糖中毒患者气道困难和气管插管失败1例报告
粘多糖病是一种罕见的溶酶体贮积病,是由参与糖胺聚糖降解的溶酶体酶缺陷引起的。不同的粘多糖病是由不同的酶缺乏引起的,麻醉并发症与受累器官有关。粘多糖病是罕见的,很少有麻醉师遇到这样的病人。我们有一例II型粘多糖病。我们尝试了几次气管插管,但我们经历了气管插管失败。由于手术时间短,我们决定在气囊面罩通气下进行手术。没有饱和时间。患者的自主呼吸功能恢复并苏醒。我们还简要讨论了II型粘多糖病患者的病理生理学、临床特征和可能的气道管理选择。
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