Doing more with less: surgical results of pediatric posterior fossa tumors from a single center in Latin America.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Child's Nervous System Pub Date : 2024-09-01 Epub Date: 2024-07-12 DOI:10.1007/s00381-024-06539-w
Cleiton Formentin, Lucas de Souza Rodrigues Dos Santos, Leo Gordiano Matias, Dayvid Leonardo de Castro Oliveira, Marcelo Ferreira Sabba, Andrei Fernandes Joaquim, Helder Tedeschi, Enrico Ghizoni
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引用次数: 0

Abstract

Objective: We aim to report the epidemiology, surgical outcomes, and survival rates of pediatric patients with posterior fossa tumors in a large single-center case series.

Methods: A retrospective analysis was conducted on pediatric patients who underwent surgical treatment for posterior fossa tumors between January 2011 and January 2019.

Results: A total of 135 pediatric patients, with an average age of 7.5 years at diagnosis and a mean follow-up of 35.7 months, were included in the study. Most tumors were located within the midline, with ventriculomegaly observed in 71.4% of the patients. Pilocytic astrocytomas encompassed the majority of tumors (34.1%), followed by medulloblastomas (27.4%) and ependymomas (11.8%). Gross total resection (GTR) was achieved in 71.8% of the patients, with a recurrence rate of 20%. Surgical complications were observed in 25.9% of the patients. GTR significantly impacted 5-year overall survival (OS) and 4-year progression-free survival (PFS) in patients with posterior fossa tumors. Patients who underwent GTR had a 5-year OS of 89.7%, compared to 72.7% for near-total resection and 70.8% for subtotal resection. The 4-year PFS for patients who underwent GTR was 82.5%, whereas it was 63.6% for patients who underwent near-total resection and 54.2% for patients who underwent subtotal resection.

Conclusion: Surgical resection remains the main treatment for pediatric posterior fossa tumors, and higher resection rates are linked to better survival outcomes. Despite limited resources for molecular diagnosis, our institution has demonstrated that a specialized neurooncological center with a high surgical volume can still achieve favorable survival outcomes for these patients.

Abstract Image

少花钱多办事:拉丁美洲单个中心的小儿后窝肿瘤手术效果。
目的我们旨在报告一个大型单中心病例系列中后窝肿瘤儿科患者的流行病学、手术结果和存活率:对 2011 年 1 月至 2019 年 1 月期间接受后窝肿瘤手术治疗的儿科患者进行回顾性分析:研究共纳入135名儿科患者,确诊时平均年龄为7.5岁,平均随访时间为35.7个月。大多数肿瘤位于中线内,71.4%的患者出现脑室肥大。大多数肿瘤为嗜酸性星形细胞瘤(34.1%),其次是髓母细胞瘤(27.4%)和上胚瘤(11.8%)。71.8%的患者实现了全切除(GTR),复发率为20%。25.9%的患者出现了手术并发症。GTR对后窝肿瘤患者的5年总生存期(OS)和4年无进展生存期(PFS)有明显影响。接受GTR的患者的5年OS为89.7%,而近全切除术为72.7%,次全切除术为70.8%。接受GTR的患者4年PFS为82.5%,而接受近全切和次全切的患者分别为63.6%和54.2%:结论:手术切除仍是治疗小儿后窝肿瘤的主要方法,较高的切除率与较好的生存预后相关。尽管用于分子诊断的资源有限,但我院的实践证明,手术量大的神经肿瘤专科中心仍能为这些患者带来良好的生存效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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