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53例腹膜后神经鞘瘤的临床分析

[Clinical analysis of 53 cases of retroperitoneal schwannoma].

作者信息

Zhou Haitao, Zhou Zhixiang, Liang Jianwei, Wang Zheng, Zhang Xingmao, Hu Junjie, Zhao Hong, Fang Yi, Huang Zhen, Wang Jian, Zeng Weigen

机构信息

Department of Abdominal Surgery, Cancer Hospital (Institute), Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, China.

Department of Abdominal Surgery, Cancer Hospital (Institute), Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, China. Email:

出版信息

Zhonghua Zhong Liu Za Zhi. 2014 Nov;36(11):867-70.

Abstract

OBJECTIVE

To explore the clinical characteristics, diagnosis and treatment regimens for retroperitoneal schwannoma.

METHODS

Clinicopathological data of 53 retroperitoneal schwannoma patients treated from January 1999 to April 2013 in our hospital were collected and analyzed using SPSS 13.0 statistical software.

RESULTS

Symptoms of the retroperitoneal schwannoma were vague and nonspecific. 12 patients had interrupted abdominal pain, 9 patients had abdominal discomfort, and only 6 patients presented with abdominal mass while 24 patients were detected by health checkup. There were some characteristics but not specific findings in imaging examination such as CT, ultrasonography and MRI, so preoperative diagnosis rate was low with only 9 patients diagnosed as retroperitoneal schwannoma and 21 patients diagnosed as neurogenic tumor. S-100 immunohistochemisty was very important in pathological diagnosis, and the patients with benign retroperitoneal schwannoma got 100% tumor specific 5-year survival after complete excision while the 5-year survival of malignant retroperitoneal schwannoma was only 50.0%.

CONCLUSIONS

Retroperitoneal schwannoma is a rare disease. Most of them are benign tumors, and complete surgical excision is the effective treatment.

摘要

目的

探讨腹膜后神经鞘瘤的临床特征、诊断及治疗方案。

方法

收集我院1999年1月至2013年4月收治的53例腹膜后神经鞘瘤患者的临床病理资料,采用SPSS 13.0统计软件进行分析。

结果

腹膜后神经鞘瘤症状不典型且无特异性。12例患者有间断性腹痛,9例患者有腹部不适,仅6例患者出现腹部肿块,24例患者通过健康体检发现。CT、超声及MRI等影像学检查有一些特征但无特异性表现,术前诊断率低,仅9例诊断为腹膜后神经鞘瘤,21例诊断为神经源性肿瘤。S-100免疫组化在病理诊断中非常重要,良性腹膜后神经鞘瘤患者完整切除后5年肿瘤特异性生存率为100%,而恶性腹膜后神经鞘瘤的5年生存率仅为50.0%。

结论

腹膜后神经鞘瘤是一种罕见疾病。大多数为良性肿瘤,完整手术切除是有效的治疗方法。

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