The role of reoperation in pediatric cerebellar pilocytic astrocytoma.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY
Journal of neurosurgery. Pediatrics Pub Date : 2024-05-17 Print Date: 2024-08-01 DOI:10.3171/2024.2.PEDS23236
Michelle M Kameda-Smith, Katherine Green, Dana L Hutton, Noor Ul Owase Jeelani, Dominic N P Thompson, Darren Hargrave, Kristian Aquilina
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引用次数: 0

Abstract

Objective: Cerebellar pilocytic astrocytomas (cPAs) in childhood have long been recognized to have a good prognosis after total resection, but the outcome after incomplete resective surgery remains largely unpredictable, with the incidence of radiological progressive disease ranging from 18% to 100%. It has been traditionally thought that gross-total resection was required for long-term survival, and small residuals were classically resected in a subsequent operation.

Methods: The authors analyzed their pediatric low-grade glioma (PLGG) database for cases treated between 1985 and 2020 and filtered for intracranial PAs, to determine what clinical or radiological factors precipitated revisional resective surgery in their single quaternary care center cohort.

Results: Using the pediatric low-grade glioma database, 283 patients were identified to have a histopathological diagnosis of intracranial PA between 1985 and 2020, of which 200 lesions were within the cerebellum (70.7%). The majority of patients with cPA were between 1 and 10 years of age (n = 145, 72.5%) without gender predominance (M/F = 99:101), usually presenting with 1 lesion (n = 197, 98.5%). Gross-total resection was achieved in 74.5% (n = 149) of initial surgeries for cPA. In patients with subtotal resection, the mean largest diameter of the postoperative residual tumor was 1.06 cm (range 0-2.95 cm). Seven patients with subtotal resection did not require a second resective intervention. In 31 patients the neuro-oncology multidisciplinary team recommended a second resection at a mean time interval of 22.9 months (range 0.13-81.6 months) from the initial surgery. Proportionally, the children who underwent multiple resections were also more likely to receive adjuvant chemo/radiotherapy. Functionally, the children in the multiple operation cohort experienced more complications of therapy including ongoing endocrinopathy, treatment-associated hearing deficit, and neurocognitive deficits.

Conclusions: Residual disease in cPA should be maintained under clinicocoradiological surveillance postoperatively with adoption of a more conservative approach when residual disease is not significantly changing over time.

再次手术在小儿小脑良性星形细胞瘤中的作用
目的:长期以来,人们一直认为儿童小脑柔细胞星形细胞瘤(cPAs)全切除后预后良好,但不完全切除手术后的预后在很大程度上仍无法预测,放射学进展性疾病的发生率从18%到100%不等。传统观点认为,大体全切除是长期生存的必要条件,小的残留物通常在随后的手术中切除:作者分析了他们的儿科低级别胶质瘤(PLGG)数据库中1985年至2020年间接受治疗并筛选出颅内PA的病例,以确定在他们的单个四级护理中心队列中,哪些临床或放射学因素促使了再次切除手术:利用儿科低级别胶质瘤数据库,在1985年至2020年期间确定了283例组织病理学诊断为颅内PA的患者,其中200例病变位于小脑(70.7%)。大多数cPA患者年龄在1至10岁之间(145人,72.5%),无性别差异(男/女=99:101),通常只有一个病灶(197人,98.5%)。74.5%(149 人)的 cPA 初次手术实现了大体全切除。在次全切除的患者中,术后残留肿瘤的平均最大直径为 1.06 厘米(范围为 0-2.95 厘米)。7名次全切除患者无需进行第二次切除手术。在31名患者中,神经肿瘤多学科团队建议进行第二次切除,平均间隔时间为首次手术后22.9个月(0.13-81.6个月)。从比例上看,接受过多次切除手术的患儿也更有可能接受辅助化疗/放疗。在功能上,多次手术队列中的患儿经历了更多的治疗并发症,包括持续的内分泌病变、治疗相关的听力障碍和神经认知障碍:结论:cPA术后残留疾病应继续接受临床放射学监测,当残留疾病随时间变化不明显时,应采取更保守的治疗方法。
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
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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