山东大学耳鼻喉眼学报 ›› 2025, Vol. 39 ›› Issue (1): 105-109.doi: 10.6040/j.issn.1673-3770.0.2023.450
王登茂,温鑫,耿江桥,张光远,刘晓峰
WANG Dengmao, WEN Xin, GENG Jiangqiao, ZHANG Guangyuan, LIU Xiaofeng
摘要: 目的 探讨儿童鼻咽部毛息肉及错构瘤的临床特点及治疗方法。 方法 回顾性分析1例来源于咽鼓管毛息肉合并鼻咽部错构瘤儿童患者的临床资料并复习相关文献,总结其临床表现、诊断、治疗方法及预后。 结果 患儿手术过程顺利,术后临床症状消失。术后病理提示来源于咽鼓管肿物为毛息肉,鼻咽部肿物为错构瘤。术后随访半年,患儿无复发。 结论 儿童咽鼓管毛息肉合并鼻咽部错构瘤为罕见病,主要表现为上呼吸道梗阻,早期诊断,尽早彻底手术是治疗该疾病的关键。
中图分类号:
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