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小儿丘脑脚肿瘤治疗中的手术及分子学考量

Surgical and molecular considerations in the treatment of pediatric thalamopeduncular tumors.

作者信息

Lee Ryan P, Foster Kimberly A, Lillard Jock C, Klimo Paul, Ellison David W, Orr Brent, Boop Frederick A

机构信息

College of Medicine, University of Tennessee Health Science Center.

Department of Neurosurgery, Le Bonheur Children's Hospital.

出版信息

J Neurosurg Pediatr. 2017 Sep;20(3):247-255. doi: 10.3171/2017.4.PEDS16668. Epub 2017 Jul 7.

Abstract

OBJECTIVE Thalamopeduncular tumors are a group of pediatric low-grade gliomas that arise at the interface of the thalamus and brainstem peduncle. They typically occur within the first 2 decades of life, presenting with progressive spastic hemiparesis. Treatment strategies, including surgical intervention, have varied significantly. The authors present their experience in the treatment of 13 children, ages 2-15 years, with non-neurofibromatosis-related pilocytic astrocytomas located in the thalamopeduncular region. METHODS Between 2003 and 2016, 13 children presenting with progressive spastic hemiparesis due to a pilocytic astrocytoma at the interface of the thalamus and cerebral peduncles were identified. Medical records were reviewed retrospectively for clinical, radiological, pathological, and surgical data. Formalin-fixed, paraffin-embedded tissue was obtained for 12 cases and tested for KIAA1549-BRAF fusion and BRAF V600E point mutation. RESULTS On preoperative diffusion tensor imaging tractography (performed in 12 patients), the ipsilateral corticospinal tract was displaced laterally in 1 case (8.3%), medially in 1 case (8.3%), anterolaterally in 10 cases (83%), and posteriorly in no cases. Ten patients underwent resection via a transtemporal, transchoroidal approach, which was chosen to avoid further damage to motor function in cases of tumors that caused anterolateral or medial corticospinal tract displacement. With this approach, complications included hemianopia, oculomotor palsy, and tremor at a rate of 50%. Among the 12 patients with obtainable follow-up (mean 50.9 months), none received adjuvant therapy, and only 2 (17%) experienced recurrence or progression. KIAA1549-BRAF fusions were present in 10 cases (83%), while BRAF V600E was absent (0%). The 2 fusion-negative tumors had clinical features atypical for the series, including multi-focality and infiltration. CONCLUSIONS Transcortical, transchoroidal resection of thalamopeduncular tumors through the middle temporal gyrus allows for a high rate of gross-total resection and cure. Diffuse tensor tractography is a critical component of the preoperative planning process to determine the location of white matter tracts in proximity. Molecular status may correlate with clinical features, and the presence of BRAF lesions offers an additional target for future novel therapeutics.

摘要

目的

丘脑脚肿瘤是一组发生于丘脑与脑干脚交界处的儿童低度胶质瘤。它们通常在生命的前20年内出现,表现为进行性痉挛性偏瘫。包括手术干预在内的治疗策略差异很大。作者介绍了他们治疗13例年龄在2至15岁之间、位于丘脑脚区域的非神经纤维瘤病相关的毛细胞型星形细胞瘤患儿的经验。方法:在2003年至2016年期间,确定了13例因丘脑与脑桥脚交界处的毛细胞型星形细胞瘤而出现进行性痉挛性偏瘫的儿童。对病历进行回顾性分析,以获取临床、放射学、病理学和手术数据。12例获取了福尔马林固定、石蜡包埋组织,并检测了KIAA1549-BRAF融合和BRAF V600E点突变。结果:在术前扩散张量成像纤维束成像(12例患者进行了此项检查)中,同侧皮质脊髓束向外移位1例(8.3%),向内移位1例(8.3%),向前外侧移位10例(83%),向后移位无病例。10例患者通过经颞叶、经脉络膜入路进行切除,对于导致皮质脊髓束向前外侧或内侧移位的肿瘤,选择该入路以避免进一步损害运动功能。采用该入路,并发症包括偏盲、动眼神经麻痹和震颤,发生率为50%。在12例可获得随访的患者中(平均50.9个月),无人接受辅助治疗,仅有2例(17%)出现复发或进展。10例(83%)存在KIAA1549-BRAF融合,而BRAF V600E均不存在(0%)。2例融合阴性肿瘤具有该系列非典型的临床特征,包括多灶性和浸润性。结论:通过颞中回经皮质、经脉络膜切除丘脑脚肿瘤可实现高比例的全切除和治愈。弥散张量纤维束成像术是术前规划过程中确定邻近白质纤维束位置的关键组成部分。分子状态可能与临床特征相关,BRAF病变的存在为未来新型治疗提供了额外靶点。

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