山东大学耳鼻喉眼学报 ›› 2023, Vol. 37 ›› Issue (3): 30-34.doi: 10.6040/j.issn.1673-3770.0.2022.150
• 论著 • 上一篇
李笑颖1,李岩2,吴允刚3,张辉3,马林祥3,赵玉凤3,孙聚兴3,张瑾1
LI Xiaoying1, LI Yan2, WU Yungang3, ZHANG Hui3, MA Linxiang3, ZHAO Yufeng3, SUN Juxing3, ZHANG Jin1
摘要: 目的 探讨鼻腔成釉细胞瘤的临床特点及治疗方法,以便于早发现早诊断。 方法 回顾性分析1例鼻腔成釉细胞瘤患者的临床资料并复习相关文献。 结果 成釉细胞瘤多发生于口腔及颌骨,发生于鼻腔鼻窦极其少见。患者可表现为鼻塞、鼻出血、鼻窦区压痛等,病情严重者可导致面部畸形。影像学检查可确定病变的范围及邻近组织关系。治疗主要采取手术彻底清除病变,可联合靶向治疗综合治疗。术后复发率高, 可恶变为成釉细胞癌。 结论 鼻腔成釉细胞瘤极其罕见,虽为良性肿瘤,但是其生物学行为具有侵袭性。患者的临床表现及影像学检查不具有特异性,需要通过病理学检查确诊。
中图分类号:
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