"我的声音听起来不一样":一种急性非发病性耳鼻缺陷病例
Rita Aldeia da Silva1, Sandra Catarina Ferraz2, Inês Barros Rua3
1Pediatrics, Hospital de Braga, Braga, PRT.
Cureus
|December 20, 2024
概括
本案例研究描述了儿童的急性异常发病性耳鼻功能缺陷,这种罕见的疾病会导致语音和吞问题. 及时诊断和治疗导致完全康复,强调了随访的重要性.
科学领域:
- 儿科耳鼻喉科 儿科耳鼻喉科
- 儿科神经学 儿科神经学
- 语音语言病理学 语音语言病理学
背景情况:
- 急性异常喉功能缺陷 (VPI) 是一种罕见的疾病,其特征是突然发作的喉功能障碍.
- 它经常表现为语言和吞困难,如鼻过高和鼻.
- 虽然它经常与病毒感染有关,但其异常性质需要彻底调查.
研究的目的:
- 报告儿科病人的急性异常发病性喉功能缺陷病例.
- 讨论这种不常见的疾病的诊断挑战和管理策略.
- 强调差异诊断和对良性结果的监测的重要性.
主要方法:
- 进行了全面的诊断检查,包括鼻喉镜检查,神经成像 (大脑和宫) 和传染病血清学.
- 患者接受了一种治疗方案,包括短时间的皮质类固醇 (普雷尼索隆) 和语音治疗.
- 临床表现,诊断结果和治疗反应都被仔细记录下来.
主要成果:
- 患者出现单侧,导致开放的鼻和鼻.
- 广泛的调查排除了结构性,神经学和传染性原因.
- 在先尼索隆治疗和语音治疗后,在一个月内实现了完全症状的消失.
结论:
- 虽然在儿童中很少见,但急性异常性喉功能缺陷可以通过医疗和治疗干预措施的结合来有效地管理.
- 这一案例凸显了排除其他潜在病因的必要性以及这种疾病的普遍有利预后.
- 持续的随访至关重要,以确认自我限制性质,并确认喉功能障碍的解决.
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