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[儿童神经母细胞瘤合并眼阵挛-肌阵挛-共济失调综合征的综合治疗]

[Comprehensive treatment of neuroblastoma in children associated with opsoclonus-myoclonus-ataxia syndrome].

作者信息

Zhao Weihong, Sun Qing, Xie Yao, Hua Ying, Xiong Hui, Jia Jun, Lu Xintian

机构信息

Department of Pediatrics, First Hospital, Peking University, Beijing 100034, China.

Email:

出版信息

Zhonghua Er Ke Za Zhi. 2014 Jul;52(7):540-3.

Abstract

OBJECTIVE

To investigate the efficacy of combined modality therapy for neuroblastoma in children associated with opsoclonus-myoclonus syndrome (OMS-NB).

METHOD

From May 2011 to December 2013, 6 consecutive patients (4 boys and 2 girls) diagnosed as OMS-NB underwent surgery and chemotherapy in the First Hospital, Peking University. The median age of onset was 19.5 months (range 13-24 months) and misdiagnosis occurred 7.5 months (range 2-14 months) ago. A retrospective analysis for the location, stage, pathological type, treatment way and outcome of neuroblastoma was done.

RESULT

(1) All patients were misdiagnosed as simply opsoclonus-myoclonus syndrome (OMS) at the time of onset. They had been receiving treatment with adrenocorticotropic hormone and intravenous immunoglobulin within 1-13 months.OMS-NB was diagnosed by means of enhanced abdominal CT image which was delayed to be given after the poor efficacy or relapse. (2) The primary tumors were almost all small, stage I-II, located in adrenal, retroperitoneal or pelvis. The pathology of tumors included ganglioneuroblastoma (5/6) and neuroblastoma (1/6). (3) All these cases underwent surgery, 4/6 cases with complete tumor resection, 2/6 cases with tumor around the aorta and induced local residue. Preoperative and postoperative chemotherapy was given to 2 and 5 cases, respectively. (4) The patients were followed up for 3-31 months, except 1 patient lost, the other 5 are currently surviving disease-free (3 having been at the end of chemotherapy, 1 still in chemotherapy, and another had local recurrence and is receiving radiotherapy and chemotherapy after the second operation and now also stopped taking the medicine). The symptoms of nervous system have been significantly improved during postoperative chemotherapy.

CONCLUSION

To reduce the misdiagnosis, regular CT imaging of the abdomen or pelvic should be ordered for all cases with OMS. The children with OMS-NB need to be actively treated with the combined modality therapy including surgery, chemotherapy or radiotherapy, to reduce recurrence and reduce the symptoms of nervous system.

摘要

目的

探讨联合治疗对小儿神经母细胞瘤合并眼阵挛-肌阵挛综合征(OMS-NB)的疗效。

方法

2011年5月至2013年12月,6例连续诊断为OMS-NB的患者(4例男孩,2例女孩)在北京大学第一医院接受手术及化疗。发病年龄中位数为19.5个月(范围13 - 24个月),误诊时间为7.5个月(范围2 - 14个月)。对神经母细胞瘤的位置、分期、病理类型、治疗方式及预后进行回顾性分析。

结果

(1)所有患者发病时均被误诊为单纯眼阵挛-肌阵挛综合征(OMS)。他们在1 - 13个月内接受了促肾上腺皮质激素及静脉注射免疫球蛋白治疗。在疗效不佳或复发后延迟行增强腹部CT检查确诊为OMS-NB。(2)原发肿瘤几乎均为小肿瘤,Ⅰ-Ⅱ期,位于肾上腺、腹膜后或盆腔。肿瘤病理包括神经节神经母细胞瘤(5/6)和神经母细胞瘤(1/6)。(3)所有病例均接受了手术,4/6例肿瘤完全切除,2/6例肿瘤位于主动脉周围并残留局部病灶。分别有2例和5例患者接受了术前及术后化疗。(4)患者随访3 - 31个月,除1例失访外,其他5例目前无病存活(3例已完成化疗,1例仍在化疗,另1例局部复发,二次手术后接受放疗及化疗,现也已停药)。术后化疗期间神经系统症状明显改善。

结论

为减少误诊,对于所有OMS患者均应常规行腹部或盆腔CT检查。OMS-NB患儿需积极采用手术、化疗或放疗等联合治疗,以减少复发并减轻神经系统症状。

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