颞骨软骨肉瘤19例临床诊断与手术疗效分析OA
Diagnosis and surgical outcomes of temporal bone chondrosarcoma
目的 探讨颞骨软骨肉瘤手术治疗效果.方法 回顾性纳入1999年8月至2022年5月于解放军总医院诊治的19例颞骨软骨肉瘤患者为研究对象,分析其临床表现、肿瘤范围、手术方式及预后情况.采用Kaplan-Meier法计算疾病特异性生存率、无病生存率,并绘制生存曲线.结果 面瘫和听力下降是颞骨软骨肉瘤患者最常见的临床症状,易误诊、漏诊,增强MRI联合薄层CT可作为鉴别诊断的核心手段.根据病变范围选择个性化治疗方案,单纯手术切除12例,手术+放疗4例,手术+放疗+化疗2例,手术+化疗1例.经乳突入路肿物切除5例,经颈-乳突入路5例,行颞骨次全切除术4例,经迷路耳囊入路1例,行颅中窝入路4例,其中4例行耳大神经移植重建面神经功能,术后病理诊断均为颞骨软骨肉瘤.术后随访1.8~23.5年,2例失访,4例复发,除2例失访外全部存活至今,术后5年总体生存率和无病生存率均为61.5%.结论 颞骨软骨肉瘤起病隐匿,影像学联合病理是确诊关键,根治性手术切除为核心治疗手段,结合辅助放疗可减少复发,长期随访(≥10年)对监测复发至关重要.
Objective To report long-term therapeutic outcomes in patients undergoing surgical management of temporal bone chondrosarcoma.Methods Clinical data of 19 patients with temporal bone chondrosarcoma treated at PLA General Hospital from August 1999 to May 2022 were retrospectively analyzed,including clinical manifestations,extent of tumor involvement,surgical approaches,and prognosis.Kaplan-Meier method was used to calculate overall survival(OS)and disease-free survival(DFS)rates.Survival curves were plotted.Results The median age of the 19 patients was 42 years(21~66 years).Common symptoms included facial paralysis and hearing loss.Diagnosis was primarily based on imaging.Individualized treatment strategies were adopted based on tumor size:12 patients underwent surgery alone,4 received surgery plus radiotherapy,2 received surgery combined with chemoradiotherapy,and 1 underwent surgery plus chemotherapy.Surgical approaches included transmastoid(n=5),cervical-transmastoid(n=5),subtotal temporal bone resection(n=4),translabyrinthine-transotic(n=1),and middle cranial fossa(n=4).Facial nerve reconstruction with great auricular nerve grafting was performed in 4 cases.Chondrosarcoma was pathologically confirmed in all cases.Two patients(10.5%)were lost to follow-up(1.8~23.5 years),and 4 experienced recurrence(22.2%,including 1 recurrence before loss to follow-up).All remaining patients survived to date.Five-year overall OS and DFS rates were 61.5%.Conclusions Temporal bone chondrosarcoma presents insidiously,and imaging combined with histopathology is essential for diagnosis.Radical surgical resection remains the cornerstone of treatment,with adjuvant radiotherapy reducing the risk of recurrence.Longitudinal surveillance beyond 10 years is critical for monitoring recurrence.
李朋;曹伟;吴楷文;唐菲;刘军
解放军总医院第六医学中心耳鼻咽喉头颈外科医学部 听觉与平衡觉全国重点实验室 耳鼻喉疾病国家临床医学研究中心 聋病教育部重点实验室 聋病防治北京市重点实验室,北京 100853||皖北煤电集团总医院耳鼻咽喉头颈外科,安徽 宿州 234011解放军总医院第六医学中心耳鼻咽喉头颈外科医学部 听觉与平衡觉全国重点实验室 耳鼻喉疾病国家临床医学研究中心 聋病教育部重点实验室 聋病防治北京市重点实验室,北京 100853解放军总医院第六医学中心耳鼻咽喉头颈外科医学部 听觉与平衡觉全国重点实验室 耳鼻喉疾病国家临床医学研究中心 聋病教育部重点实验室 聋病防治北京市重点实验室,北京 100853解放军总医院第六医学中心耳鼻咽喉头颈外科医学部 听觉与平衡觉全国重点实验室 耳鼻喉疾病国家临床医学研究中心 聋病教育部重点实验室 聋病防治北京市重点实验室,北京 100853解放军总医院第六医学中心耳鼻咽喉头颈外科医学部 听觉与平衡觉全国重点实验室 耳鼻喉疾病国家临床医学研究中心 聋病教育部重点实验室 聋病防治北京市重点实验室,北京 100853
颞骨软骨肉瘤手术切除复发预后
temporal bonechondrosarcomasurgical resectionrecurrenceprognosis
《中华耳科学杂志》 2026 (9)
840-843,4
蚌埠医科大学科技项目自然科学重点项目(2023byzd263)
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