著名的囊性纤维化病例中的“Arnold Chiari畸形”的麻醉处理

Gholamreza Mohseni, F. Behnaz, Houman Teymourian, S. O. Yazdani
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引用次数: 0

摘要

囊性纤维化(CF)是一种由常染色体隐性氯通道缺陷引起的遗传病,是肺、胰腺、肝脏、肠、汗腺和附睾等器官上皮细胞中氯(Cl)通过质膜运输的生理和功能障碍。这些病例的围手术期呼吸并发症很重要。我们提出了一种麻醉方法,在24岁的男性CF病例接受全身麻醉的Arnold Chiari畸形手术。
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 "Arnold Chiari Malformation" in the well-known Case of Cystic Fibrosis
Cystic fibrosis (CF) is a genetic disease resulting from a chlorine channel defect with autosomal recessive show, a physical and functional disorder in the transport of chlorine (Cl) through the plasma membrane in epithelial cells in organs such as the lungs, pancreas, liver, intestines, sweat glands, and epididymis. These cases are important for their perioperative respiratory complications. We present an anesthesia method conducted on a 24-year-old men CF case receiving general anesthesia for Arnold Chiari malformation surgery.
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