[Anesthesia for an Eleven Year Old Girl with Sjögren-Larsson Syndrome].

Yasuyoshi Sakurai, Michiko Uchida
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Abstract

Sjögren-Larsson syndrome (SLS) is an autosomal recessive disease characterized by a triad of congenital ichthyosis, spastic quadriplegia and mental retardation. An 11-year-old girl (body weight 30 kg) diagnosed as SLS was admitted with Benett fracture of the right thumb. She was monitored with standard protocol. General anesthesia was induced by rapid induction method with propofol 50 mg and rocuronium 0.6 mg - kg⁻¹. She was ventilated with bag and mask, and intu- bated without difficulty. Neuromuscular function was continuously assessed by 40 mA-TOF-stimulation re- sponses with acceleromyography immediately after induction of general anesthesia by TOF-Watch® SX (Organon Ireland, division of MSD, Ireland). Anesthe- sia was maintained with total intravenous anesthesia with propofol 6-8-10 mg⁻¹ · hr⁻¹ in oxygen. No abnor- mal responses were observed by TOF-Watche SX despite the neuromuscular disease. Residual effect of the neuromuscular blocking agent was successfully reversed by sugammadex and she was extubated without any respiratory trouble. She was discharged on the postoperative day 1 without complications.

[一名患有Sjögren-Larsson综合征的11岁女孩的麻醉]。
Sjögren-Larsson综合征(SLS)是一种常染色体隐性遗传病,以先天性鱼鳞病、痉挛性四肢瘫痪和智力低下为特征。一名11岁女孩(体重30公斤)诊断为SLS,因右拇指Benett骨折入院。她接受了标准的监护。采用快速诱导法,用异丙酚50 mg、罗库溴铵0.6 mg - kg(⁻¹)诱导全身麻醉。她用呼吸袋和口罩进行了通气,并毫无困难地进行了插管。采用TOF-Watch®SX (Organon Ireland, MSD分部,Ireland)在全麻诱导后立即用40个ma - tof刺激反应和加速肌图持续评估神经肌肉功能。麻醉维持在全静脉麻醉下,用异丙酚6-8-10 mg(⁻¹·hr)加氧。尽管存在神经肌肉疾病,但tof - watch SX未观察到异常反应。神经肌肉阻滞剂的残余作用被糖麦德成功逆转,患者拔管后无任何呼吸问题。术后第1天出院,无并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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