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可切除的小儿肋骨尤因肉瘤的治疗结果

Outcome of resectable pediatric Ewing sarcoma of the ribs.

作者信息

Ahmed Gehad, Zamzam Manal, Zaghloul Mohamed S, Kamel Ahmed, Soliman Ranin, Zaky Iman, Salama Asmaa, Kamal Nehal, ElShafiey Maged

机构信息

Surgical Oncology Department, Children's Cancer Hospital (CCHE), 57357, Egypt; Faculty of Medicine, Helwan University, Egypt.

Pediatric Oncology Department, CCHE, Egypt; National Cancer Institute, Cairo University, Egypt.

出版信息

J Egypt Natl Canc Inst. 2017 Jun;29(2):99-104. doi: 10.1016/j.jnci.2017.03.002. Epub 2017 Apr 24.

Abstract

PURPOSE

Was to evaluate the outcome of multimodality treatment in resectable primary Ewing sarcoma/primitive neuroectodermal tumor ES/PNET of the ribs and role of thoracoscopy in facilitating resection of these tumors.

PATIENTS AND METHODS

This was a retrospective study including 22 patients with primary ES/PNET of the ribs surgically treated at Children's Cancer Hospital Egypt (CCHE) between January 2008 until the end of December 2014.

RESULTS

Median age was 8.5years (range 5months to 16years.). All patients received neoadjuvant chemotherapy. Thoracoscopic exploration was performed in 15 (68%) patients. Resection included 1,2,3 and 4 ribs in (7,4,8 and 3 patients) respectively, parts of the diaphragm (3 patients), wedge resection of the lung (10 patients) and pleural nodules (2 patients). Primary closure was feasible in 11 patients and rib transposition was done in one patient. Reconstruction by proline mesh covered by muscle flap was done in 10 patients. Margins were microscopically positive in 3 patients and close in 2 patients. Postoperative radiotherapy was given in 8 patients. With a median follow-up of 38.5months, the 3-year event -free survival (EFS) and overall survival(OS) rates were 31.6% and 55.6%, respectively.

CONCLUSION

Multimodality treatment is essential in the management of ES-PNET of the ribs. Neoadjuvant chemotherapy facilitates adequate resection. The role of thoracoscopy and the indications of postoperative radiotherapy need further evaluation.

摘要

目的

评估多模式治疗可切除的原发性肋骨尤文肉瘤/原始神经外胚层肿瘤(ES/PNET)的疗效以及胸腔镜在促进这些肿瘤切除中的作用。

患者与方法

这是一项回顾性研究,纳入了2008年1月至2014年12月底在埃及儿童癌症医院(CCHE)接受手术治疗的22例原发性肋骨ES/PNET患者。

结果

中位年龄为8.5岁(范围5个月至16岁)。所有患者均接受了新辅助化疗。15例(68%)患者进行了胸腔镜探查。切除的肋骨分别为1根、2根、3根和4根的患者有7例、4例、8例和3例,部分膈肌切除(3例),肺楔形切除(10例),胸膜结节切除(2例)。11例患者可行一期缝合,1例患者进行了肋骨移位。10例患者采用肌瓣覆盖的脯氨酸网片进行重建。3例患者显微镜下切缘阳性,2例患者切缘接近。8例患者术后接受了放疗。中位随访38.5个月,3年无事件生存率(EFS)和总生存率(OS)分别为31.6%和55.6%。

结论

多模式治疗对于肋骨ES-PNET的管理至关重要。新辅助化疗有助于充分切除。胸腔镜的作用以及术后放疗的指征需要进一步评估。

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