一名患有先天性四肢和面部挛缩、张力低下和发育迟缓综合征的9岁女孩的麻醉处理:肌腱手术期间气道困难和术后呼吸暂停。

Anesthesia and pain medicine Pub Date : 2025-01-01 Epub Date: 2025-01-25 DOI:10.17085/apm.24107
Jessica G Santos, Alexandre C Buffon
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引用次数: 0

摘要

背景:本病例报告描述了一位被诊断为先天性四肢和面部挛缩、张力低下和发育迟缓(CLIFAHDD)综合征的患者接受右手肌腱切开术的麻醉处理和术后挑战。该综合征以面部畸形、肌肉骨骼异常和呼吸障碍(包括中枢呼吸暂停)为特征,是由NALCN基因突变引起的。目的:一名确诊为cliahdd综合征的9岁女孩接受了右手肌腱的肌腱切开术。给予全身麻醉。尽管术中情况稳定,但患者在拔管后出现多次呼吸暂停,通气不足,需要使用面罩辅助通气。结论:本病例强调了CLIFAHDD综合征患者麻醉管理的挑战和注意事项,强调需要量身定制的方法和警惕的术后监测,以减轻与这种罕见遗传疾病相关的潜在呼吸并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anesthetic management of a 9-year-old girl with Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay syndrome: airway difficulties and postoperative apnea during tendon surgery.

Background: This case report described the anesthetic management and postoperative challenges of a patient diagnosed with Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay (CLIFAHDD) syndrome who underwent tenomyotomy of the right hand tendons. This syndrome, characterized by facial dysmorphisms, musculoskeletal abnormalities, and respiratory disturbances, including central apnea, is caused by a mutation in the NALCN gene.

Purpose: A 9-year-old girl diagnosed with CLIFAHDD syndrome underwent tenomyotomy of the right hand tendon. General anesthesia was administered. Despite stable intraoperative conditions, the patient experienced inadequate ventilation with multiple episodes of apnea after extubation, necessitating assisted ventilation using a face mask.

Conclusions: This case highlights the challenges and considerations in the anesthetic management of patients with CLIFAHDD syndrome, emphasizing the need for tailored approaches and vigilant postoperative monitoring to mitigate the potential respiratory complications associated with this rare genetic disorder.

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