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鼻窦腺样囊性癌的治疗结果:来自单一机构的30例病例

Treatment outcomes of sinonasal adenoid cystic carcinoma: 30 cases from a single institution.

作者信息

Seong Sang Yeob, Hyun Dong Woo, Kim Yoo Suk, Cho Hyung-Ju, Lee Jeung-Gweon, Yoon Joo-Heon, Kim Chang-Hoon

机构信息

Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea.

Department of Otorhinolaryngology, Kang-Dong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Republic of Korea.

出版信息

J Craniomaxillofac Surg. 2014 Jul;42(5):e171-5. doi: 10.1016/j.jcms.2013.08.002. Epub 2013 Sep 9.

Abstract

OBJECTIVE

To establish the clinical features and prognostic factors of sinonasal adenoid cystic carcinoma (ACC).

MATERIAL AND METHODS

Thirty patients with histopathological diagnosis of sinonasal ACC who were treated at Severance Hospital between 1990 and 2010 were included in this retrospective chart review study.

RESULTS

The 5-year disease-specific survival and disease-free survival rates were 75.3% and 37.2%, respectively. The maxillary sinus (63.3%) and nasal cavity (23.3%) were the most common sites of primary tumour. Most patients were diagnosed with advanced-stage (III/IV) disease (80.0%) and had undergone surgery and postoperative radiotherapy (70.0%). The most common histopathological subtype was cribriform type (40.9%). Local recurrence rate and distant metastasis rates were 26.7% and 23.3%, respectively. The mean time from primary treatment to recurrence was 44.5 months. Sinonasal ACC patients with stage IV and T4 disease had significantly worse survival than those with low stage and T disease. Patients with local recurrence had worse disease-specific survival than those with distant recurrence. Distant metastasis was associated with disease-free survival but not disease-specific survival.

CONCLUSION

Despite the frequent occurrence of distant metastasis, early diagnosis and effective local control seemed to be the most important factors influencing the survival of sinonasal ACC.

摘要

目的

明确鼻窦腺样囊性癌(ACC)的临床特征及预后因素。

材料与方法

本回顾性病历审查研究纳入了1990年至2010年间在Severance医院接受治疗、经组织病理学诊断为鼻窦ACC的30例患者。

结果

5年疾病特异性生存率和无病生存率分别为75.3%和37.2%。原发肿瘤最常见的部位是上颌窦(63.3%)和鼻腔(23.3%)。大多数患者被诊断为晚期(III/IV期)疾病(80.0%),且接受了手术及术后放疗(70.0%)。最常见的组织病理学亚型是筛状型(40.9%)。局部复发率和远处转移率分别为26.7%和23.3%。从初次治疗到复发的平均时间为44.5个月。IV期和T4期鼻窦ACC患者的生存率明显低于低分期和T分期患者。局部复发患者的疾病特异性生存率低于远处复发患者。远处转移与无病生存率相关,但与疾病特异性生存率无关。

结论

尽管远处转移频繁发生,但早期诊断和有效的局部控制似乎是影响鼻窦ACC患者生存的最重要因素。

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