Coca H A, Cebula H, Benmekhbi M, Chenard M P, Entz-Werle N, Proust F
Service de neurochirurgie CHU Hautepierre, 67098, Strasbourg cedex, France.
Service de neurochirurgie CHU Hautepierre, 67098, Strasbourg cedex, France.
Neurochirurgie. 2016 Dec;62(6):327-331. doi: 10.1016/j.neuchi.2016.07.005. Epub 2016 Oct 27.
Diffuse intrinsic pontine gliomas (DIPG) constitute 10-15% of all brain tumors in the pediatric population; currently prognosis remains poor, with an overall survival of 7-14 months. Recently the indication of DIPG biopsy has been enlarged due to the development of molecular biology and various ongoing clinical and therapeutic trials. Classically a biopsy is performed using a stereotactic frame assisted procedure but the workflow may sometimes be heavy and more complex especially in children. In this study the authors present their experience with frameless robotic-guided biopsy of DIPG in a pediatric population.
Retrospective study on a series of five consecutive pediatric patients harboring DIPG treated over a 4-year period. All patients underwent frameless robotic-guided biopsy via a transcerebellar approach.
Among the 5 patients studied 3 were male and 2 female with a median age of 8.6 years [range 5 to 13 years]. Clinical presentation included ataxia, hemiparesis and cranial nerve palsy in all patients. MRI imaging of the lesion showed typical DIPG features (3 of them located in the pons) with hypo-intensity on T1 and hyper-intensity signal on T2 sequences and diffuse gadolinium enhancement. The mean procedure time was 56minutes (range 45 to 67minutes). No new postoperative neurological deficits were recorded. Histological diagnosis was achieved in all cases as follows: two anaplastic astrocytomas (grade III), two glioblastomas, and one diffuse astrocytoma (grade III).
Frameless robotic assisted biopsy of DIPG in pediatric population is an easier, effective, safe and highly accurate method to achieve diagnosis.
弥漫性脑桥内在型胶质瘤(DIPG)占儿童脑肿瘤总数的10%-15%;目前预后仍然很差,总生存期为7-14个月。最近,由于分子生物学的发展以及各种正在进行的临床和治疗试验,DIPG活检的适应证有所扩大。传统上,活检是在立体定向框架辅助下进行的,但操作流程有时可能繁琐且更复杂,尤其是在儿童中。在本研究中,作者介绍了他们在儿科患者中使用无框架机器人引导活检DIPG的经验。
对连续4年治疗的5例患有DIPG的儿科患者进行回顾性研究。所有患者均通过经小脑入路接受无框架机器人引导活检。
在研究的5例患者中,3例为男性,2例为女性,中位年龄为8.6岁[范围5至13岁]。所有患者的临床表现包括共济失调、偏瘫和颅神经麻痹。病变的MRI成像显示典型的DIPG特征(其中3例位于脑桥),T1加权像呈低信号,T2加权像呈高信号,并伴有弥漫性钆增强。平均手术时间为56分钟(范围45至67分钟)。术后未记录到新的神经功能缺损。所有病例均获得组织学诊断,结果如下:2例间变性星形细胞瘤(III级),2例胶质母细胞瘤,1例弥漫性星形细胞瘤(III级)。
在儿科患者中,无框架机器人辅助活检DIPG是一种更简便、有效、安全且高度准确的诊断方法。