Edward B. Singleton Department of Radiology, Section of Pediatric Neuroradiology, Texas Children's Hospital, Houston, TX.
Department of Neuropsychology, Kennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, MD.
J Neuroimaging. 2020 Mar;30(2):192-197. doi: 10.1111/jon.12686. Epub 2020 Jan 6.
Posterior fossa syndrome (PFS), characterized by loss of language and other neurological impairments within the immediate postoperative period, occurs in approximately 25% of children who undergo surgical resection of posterior fossa tumors. Diffusion tensor imaging connectomics offer promise for elucidation of pathway-level disruption in neural connectivity of patients with this disorder. We aim to determine differences in pre- and postoperative connectomics between children with PFS and children with mild or no language deficit after surgery.
Pre- and postoperative diffusion tensor imaging connectomics were applied and compared among patients with PFS, mild deficits, and intact language.
A total of 35 patients were included in the study. Twenty-three patients with preoperative data and 24 patients with postoperative data were included in the analysis. Mean ages: PFS-8.5 years, mild-3.1 years, intact language-9.4 years (P = .02). Diagnoses included medulloblastoma (44.1%), pilocytic astrocytoma (28.6%), ependymoma (8.6%), other (11.4%), and unknown (8.6%). Five (21.7%) patients had PFS, 4 (17.4%) had mild deficits, and 14 (60.9%) had intact language. The assortativity coefficient was significantly higher in patients with PFS when compared to patients with mild deficits (P = .023). In the connectometry analyses, decreased connectivity was found involving the corpus callosum, right corticothalamic pathway, and right corticostriatal pathway in patients with PFS when compared to patients with intact language.
Our findings revealed significant differences in preoperative neural connectivity involving the corticothalamic and other pathways among children who did, versus who did not, develop PFS postoperatively. Diffusion tensor imaging connectomics offers a unique opportunity to study the effect of the posterior fossa tumors on cerebello-cerebral networks and provide new insights into the mechanism of the structural plasticity/reorganization after surgery.
术后即刻出现语言丧失和其他神经功能障碍的后颅窝综合征(PFS),约发生于 25%接受后颅窝肿瘤切除术的儿童中。弥散张量成像连接组学有望阐明该疾病患者的神经连接通路水平破坏。我们旨在确定 PFS 患儿与术后语言轻度受损或无语言损伤患儿的术前和术后连接组学差异。
对 PFS 患儿、语言轻度受损患儿和语言完整患儿进行术前和术后弥散张量成像连接组学检查并进行比较。
本研究共纳入 35 例患者。23 例患者具有术前数据,24 例患者具有术后数据。患者平均年龄:PFS-8.5 岁,轻度-3.1 岁,语言完整-9.4 岁(P =.02)。诊断包括髓母细胞瘤(44.1%)、毛细胞星形细胞瘤(28.6%)、室管膜瘤(8.6%)、其他(11.4%)和未知(8.6%)。5 例(21.7%)患者发生 PFS,4 例(17.4%)患者出现轻度语言障碍,14 例(60.9%)患者语言完整。与语言轻度受损患儿相比,PFS 患儿的配价系数明显更高(P =.023)。在连接分析中,与语言完整患儿相比,PFS 患儿的胼胝体、右侧皮质丘脑通路和右侧皮质纹状体通路的连接性降低。
我们的研究结果表明,术后发生 PFS 的患儿与未发生 PFS 的患儿在术前神经连接方面存在显著差异,涉及皮质丘脑和其他通路。弥散张量成像连接组学为研究后颅窝肿瘤对小脑-大脑网络的影响提供了独特的机会,并为术后结构重塑/重组的机制提供了新的见解。