山东大学耳鼻喉眼学报 ›› 2025, Vol. 39 ›› Issue (4): 186-192.doi: 10.6040/j.issn.1673-3770.0.2024.297
石金莲1,李建兴1,黄幼生2,林铭轩3,刘灵云1,卢永田4
SHI Jinlian1, LI Jianxing1, HUANG Yousheng2, LIN Mingxuan3, LIU Lingyun1, LU Yongtian4
摘要: 炎性肌纤维母细胞瘤(inflammatory myofibroblastic tumor, IMT)是一种罕见的间叶源性肿瘤,好发于肺部,喉部发生较为少见。喉部IMT的临床表现通常包括声音嘶哑和呼吸困难等,但由于这些症状的非特异性,喉部IMT容易被误诊为其他喉部疾病。病理学特征显示,喉部IMT主要由巨细胞、浆细胞、淋巴细胞等炎症细胞以及纺锤形肿瘤细胞组成,后者呈现光滑肌肉细胞或肌成纤维细胞的表型,且具有不同程度的细胞密集区和血管分布。确诊喉部IMT依赖于影像学检查、病理学评估及免疫组化检测的综合应用。手术切除是治疗喉部IMT的首选方法,对于无法手术或存在复发转移的病例,ALK抑制剂等靶向治疗显示出潜在的治疗效果。肿瘤的大小、分期及切除范围是影响预后的重要因素。本文综述了喉部IMT的发病机制、临床特征、诊断方法及治疗策略等方面的最新研究进展,有助于提高喉部IMT的诊断准确率和治疗效果。
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