Evolution of Surgical Management of Pineal Region Tumors in the Pediatric Population: A 17-Year Experience at a Single Institution.

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY Pediatric Neurosurgery Pub Date : 2024-01-01 Epub Date: 2024-04-26 DOI:10.1159/000538745
Nirali Patel, Alexandria Marino, Tianzhi Tang, Kelsi Chesney, Jean Paul Bryant, Trae Robison, Robert F Keating, John S Myseros, Hasan R Syed
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Abstract

Introduction: Pineal region tumors have historically been challenging to treat. Advances in surgical techniques have led to significant changes in care and outcomes for these patients, and this is well demonstrated by our single institution's experience over a 17-year-period in which the evolution of diagnosis, treatment, and outcomes of pineal tumors in pediatric patients will be outlined.

Methods: We retrospectively collected data on all pediatric patients with pineal region lesions treated with surgery at Children's National Hospital (CNH) from 2005 to 2021. Variables analyzed included presenting symptoms, presence of hydrocephalus, diagnostic and surgical approach, pathology, and adverse events, among others. IRB approval was obtained (IRB: STUDY00000009), and consent was waived due to minimal risk to patients included.

Results: A total of 43 pediatric patients with pineal region tumors were treated during a 17-year period. Most tumors in our series were germinomas (n = 13, 29.5%) followed by pineoblastomas (n = 10, 22.7%). Twenty seven of the 43 patients (62.8%) in our series received a biopsy to establish diagnosis, and 44.4% went on to have surgery for resection. The most common open approach was posterior interhemispheric (PIH, transcallosal) - used for 59.3% of the patients. Gross total resection was achieved in 50%; recurrence occurred in 20.9% and mortality in 11% over a median follow-up of 47 months. Endoscopic third ventriculostomy (ETV) was employed to treat hydrocephalus in 26 of the 38 patients (68.4%) and was significantly more likely to be performed from 2011 to 2021. Most (73%) of the patients who received an ETV also underwent a concurrent endoscopic biopsy. No difference was found in recurrence rate or mortality in patients who underwent resection compared to those who did not, but complications were more frequent with resection. There was disagreement between frozen and final pathology in 18.4% of biopsies.

Conclusion: This series describes the evolution of surgical approaches and outcomes over a 17-year-period at a single institution. Complication rates were higher with open resection, reinforcing the safety of pursuing endoscopic biopsy as an initial approach. The most significant changes occurred in the preferential use of ETVs over ventriculoperitoneal shunts. Though there has been a significant evolution in our understanding of and treatment for these tumors, in our series, the outcomes for these patients have not significantly changed over that time.

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小儿松果体区肿瘤手术治疗的演变:一家医疗机构 17 年的经验。
简介松果体区肿瘤的治疗历来具有挑战性。手术技术的进步使这些患者的治疗和预后发生了重大变化,我们一家医疗机构 17 年来的经验充分证明了这一点,我们将概述儿科松果体肿瘤诊断、治疗和预后的演变过程:我们回顾性地收集了 2005-2021 年间在国立儿童医院(CNH)接受手术治疗的所有松果体区病变儿科患者的数据。分析的变量包括表现症状、是否存在脑积水、诊断和手术方法、病理和不良事件等。该研究已获得国际注册研究委员会(IRB)批准(IRB:STUDY00000009),由于对纳入患者的风险极小,因此无需征得同意:结果:17年间,共有43名患有松果体区肿瘤的儿童患者接受了治疗。在我们的系列研究中,大多数肿瘤是生殖细胞瘤(13 例,占 29.5%),其次是松果体母细胞瘤(10 例,占 22.7%)。在我们的系列研究中,43名患者中有27人(62.8%)接受了活组织检查以确定诊断,44.4%的患者接受了手术切除。59.3%的患者采用了最常见的开放手术方式,即大脑半球后部(PIH,经胼胝体)切除术。在中位随访47个月期间,50%的患者实现了大体全切除;20.9%的患者复发,11%的患者死亡。38例患者中有26例(68.4%)采用了内镜下第三脑室造口术(ETV)治疗脑积水,而且在2011-2021年期间采用这种手术的几率明显增加。大多数(73%)接受 ETV 的患者还同时进行了内镜活检。接受切除术的患者与未接受切除术的患者在复发率或死亡率方面没有差异,但切除术的并发症发生率更高。18.4%的活检结果与最终病理结果不一致:该系列研究描述了一家医疗机构在17年间手术方法和结果的演变。开放性切除术的并发症发生率较高,这加强了将内窥镜活检作为初始方法的安全性。最重要的变化发生在优先使用脑室腹腔分流术(ETV)方面。虽然我们对这些肿瘤的认识和治疗方法有了很大的发展,但在我们的系列研究中,这些患者的预后并没有发生显著变化。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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