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[头颈部滑膜肉瘤——39例回顾性研究]

[Synovial sarcoma of the head and neck--a retrospective study of 39 cases].

作者信息

Li Wen, Yang Liu, Li Qiong, Chen Min, Zhang Hongying

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Nov;27(21):1167-70.

Abstract

OBJECTIVE

Synovial sarcoma (SS) of the head and neck is rare in comparison with those took place in the extremities. This study was planned to investigate the relationship between pathological diagnosis, tumor location and clinical outcome of SS of the head and neck.

METHOD

Thirty-nine cases of SS in head and neck hospitalized in West China Hospital from 1966 to 2011 was retrospectively studied by reviewing the medical record data, the pathological slices of the operative specimen and followed-up from 1 to 192 months with the mean time of 43.2 months postoperatively. The parameters of clinical outcome were focused on the time to first recurrence after primary surgery and follow-up time. The reviewed results were statistically processed.

RESULT

The age of the patients ranged from 8 to 66 years old with the median age of 35, among them 27 are males. Pathologically, 18 cases are biphasic, 17 cases are monophasic and 3 cases are low-differentiated SS. 4 cases were proved by cytogenetic methods of either fluorescence in situ hybridization(FISH) or RT-PCR. 23 cases experienced repeated recurrence with the most up to 4 times operations after sole surgical approach. Only one lymphatic metastasis was suspected in all. 16 patients got adjuvant radiotherapy or chemotherapy. 4 patients died but only one death was associated directly with SS recurrence. There was no significant relationship between pathological subtype and recurrence (Fisher's Exact Test P-value > 0.05), no significant relationship between tumor location and recurrence (Fisher's Exact Test P-value > 0.05).

CONCLUSION

SS of head and neck is a special entity that has potential of easy recurrence but good prognosis. Surgery should still be the primary treatment approach. Cytogenetic methods are recommended to as certain the diagnosis in order to choose reasonable treatment protocols.

摘要

目的

与发生于四肢的滑膜肉瘤相比,头颈部滑膜肉瘤较为罕见。本研究旨在探讨头颈部滑膜肉瘤的病理诊断、肿瘤部位与临床结局之间的关系。

方法

回顾性研究1966年至2011年在华西医院住院的39例头颈部滑膜肉瘤患者的病历资料、手术标本病理切片,并进行1至192个月的随访,术后平均随访时间为43.2个月。临床结局参数重点关注初次手术后首次复发时间和随访时间。对回顾结果进行统计学处理。

结果

患者年龄8至66岁,中位年龄35岁,其中男性27例。病理上,双相型18例,单相型17例,低分化滑膜肉瘤3例。4例通过荧光原位杂交(FISH)或逆转录聚合酶链反应(RT-PCR)等细胞遗传学方法得以确诊。23例出现反复复发,单纯手术治疗后最多接受4次手术。仅怀疑有1例发生淋巴结转移。16例患者接受了辅助放疗或化疗。4例患者死亡,但仅1例死亡与滑膜肉瘤复发直接相关。病理亚型与复发之间无显著关系(Fisher精确检验P值>0.05),肿瘤部位与复发之间无显著关系(Fisher精确检验P值>0.05)。

结论

头颈部滑膜肉瘤是一种特殊的疾病,具有易复发但预后良好的特点。手术仍应作为主要治疗方法。建议采用细胞遗传学方法明确诊断,以便选择合理的治疗方案。

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