小儿后窝外侧型脑膜瘤

Pablo Miranda-Lloret, Estela Plaza-Ramírez, Juan Antonio Simal-Julián, Giovanni Pancucci, Adela Cañete, Alejandro Montoya-Filardi, Gemma Llavador
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摘要

背景:外侧型后窝外胚瘤在临床和病理上都是一种定义明确的亚型肿瘤,预后较差。其发病率较低,手术治疗具有挑战性。本研究的目的是回顾我们的外侧型后窝外胚瘤系列研究,并将我们的研究结果与之前的系列研究结果进行比较:方法:在过去十年中,我们儿科接诊了 30 例外胚骺瘤患者,其中有 7 例为外侧型后窝外胚骺瘤。然后,我们进行了一项回顾性、描述性研究:结果:患者平均年龄为 3.75 岁。6例患者出现脑积水。确诊时的平均肿瘤体积为 61 毫升。6例患者实现了完全切除,1例患者接近完全切除。5 名患者暂时需要进行胃造口术和气管造口术。平均随访时间为 58 个月。在此期间,1 例患者病情恶化,最终死亡。4 例脑积水患者需要进行脑室腹腔 CSF 分流术,2 例患者进行了第三脑室造口术。在最后的随访中,根据兰斯基量表,4 例患者生活正常,2 例出现轻度限制:结论:外侧型后窝外胚瘤手术治疗的目的是完全切除肿瘤。与下颅神经功能障碍相关的神经功能缺损很常见,但都是一过性的。对这些肿瘤进行更深入的基因鉴定可能会发现风险因素,为分层辅助治疗提供指导。
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Lateral-type posterior fossa ependymomas in pediatric population

Background

Lateral-type posterior fossa ependymomas are a well-defined subtype of tumours both clinically and pathologically, with a poor prognosis. Their incidence is low and surgical management is challenging. The objective of the present work is to review our series of lateral-tye posterior fossa ependymomas and compare our results with those of previous series.

Methods

Among 30 cases of ependymoma operated in our paediatric department in the last ten years, we identified seven cases of lateral-type posterior fossa ependymomas. We then performed a retrospective, descriptive study.

Results

Mean age of our patients was 3.75 years. 6 cases presented with hydrocephalus. Mean tumour volume at diagnosis was 61 cc. A complete resection was achieved in six cases and a near-total resection in one patient. 5 patients transiently required a gastrostomy and a tracheostomy. Mean follow-up was 58 months. One case progressed along this period and eventually died. 4 cases of hydrocephalus required a ventriculoperitoneal CSF shunt and two were managed with a third ventriculostomy. At last follow-up 4 patients carried a normal life and two displayed a mild restriction according to Lansky´s scale.

Conclusions

The aim of surgical treatment in lateral-type posterior fossa ependymomas is complete resection. Neurological deficits associated to lower cranial nerve dysfunction are common but transient. Deeper genetic characterization of these tumours may identify risk factors that guide stratification of adjuvant therapies.

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