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颞骨及侧颅底恶性肿瘤:81例患者的经验与结果

Temporal bone and lateral skull base malignancy: experience and results with 81 patients.

作者信息

Manolidis S, Pappas D, Von Doersten P, Jackson C G, Glasscock M E

机构信息

The Bobby R. Alford Department of Otolaryngology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Am J Otol. 1998 Nov;19(6 Suppl):S1-15.

PMID:9827809
Abstract

OBJECTIVE

This study aimed to examine predictive factors and treatment outcome and to devise a staging method for malignant lateral skull base disease.

STUDY DESIGN

The study design was a retrospective review of all lateral skull base surgery cases.

SETTING

The study was conducted at a tertiary referral center.

PATIENTS

Of 317 lateral skull base lesions, 81 patients were found to have malignant disease. Three groups were identified, and the data were analyzed according to the following: epithelial malignancies, 30 patients; malignancies of salivary gland origin, 23 patients; and malignancies of mesenchymal origin, 28 patients. The mean age was 48.5 years with a range of 5-83 years. There were 42 males and 39 females. Our mean follow-up time was 54 months with a range of 1-180 months. Forty-three patients were alive without evidence of recurrent disease, 6 were living with disease, 25 were dead of disease, 3 died of other causes, and 4 were lost to follow-up.

INTERVENTIONS

All patients underwent surgery with curative intent. Forty-two received adjuvant radiation, and 8 received chemotherapy.

MAIN OUTCOME MEASURES

Treatment failure, survival, cranial nerve deficits, complications, and predictive factors were analyzed.

RESULTS

A 58% treatment success rate was observed. Epithelial and salivary malignancy had a poorer prognosis, and pain and facial nerve dysfunction at presentation carried a worse prognosis.

CONCLUSIONS

Lateral skull base malignancy is a rare entity that continues to challenge cranial base surgeons. Cranial nerve deficits and complications are frequent. The success rate of treatment is dependent on histology and disease extent.

摘要

目的

本研究旨在探讨恶性侧颅底疾病的预测因素和治疗结果,并设计一种分期方法。

研究设计

本研究设计为对所有侧颅底手术病例进行回顾性分析。

研究地点

本研究在一家三级转诊中心进行。

患者

在317例侧颅底病变中,81例被发现患有恶性疾病。分为三组,并根据以下情况分析数据:上皮性恶性肿瘤30例;涎腺源性恶性肿瘤23例;间叶源性恶性肿瘤28例。平均年龄为48.5岁,范围为5至83岁。男性42例,女性39例。我们的平均随访时间为54个月,范围为1至180个月。43例患者存活且无疾病复发迹象,6例带瘤生存,25例死于疾病,3例死于其他原因,4例失访。

干预措施

所有患者均接受了根治性手术。42例接受了辅助放疗,8例接受了化疗。

主要观察指标

分析治疗失败、生存、颅神经功能缺损、并发症及预测因素。

结果

观察到治疗成功率为58%。上皮性和涎腺恶性肿瘤预后较差,就诊时疼痛和面神经功能障碍预后更差。

结论

侧颅底恶性肿瘤是一种罕见疾病,持续挑战颅底外科医生。颅神经功能缺损和并发症很常见。治疗成功率取决于组织学类型和疾病范围。

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