Harreld J H, Hwang S N, Qaddoumi I, Tatevossian R G, Li X, Dalton J, Haupfear K, Li Y, Ellison D W
From the Departments of Diagnostic Imaging (J.H.H., S.N.H.)
From the Departments of Diagnostic Imaging (J.H.H., S.N.H.).
AJNR Am J Neuroradiol. 2016 Dec;37(12):2370-2375. doi: 10.3174/ajnr.A4892. Epub 2016 Jul 28.
Pilocytic astrocytomas, the most common posterior fossa tumors in children, are characterized by KIAA1549-BRAF fusions and shows excellent 5-year survival rates. Pilocytic astrocytoma with gangliocytic differentiation, a recently defined pilocytic astrocytoma variant that includes glial and neuronal elements similar to a ganglioglioma, may be distinguished from a classic ganglioglioma by molecular, radiologic, and histopathologic features. This study investigated whether imaging could distinguish posterior fossa pilocytic astrocytoma with and without gangliocytic differentiation.
Preoperative MRIs (± CTs) of 41 children (age range, 7 months to 15 years; mean age, 7.3 ± 3.7 years; 58.5% male) with pilocytic astrocytoma with gangliocytic differentiation (n = 7) or pilocytic astrocytoma (n = 34) were evaluated; differences in tumor location, morphology, and minimum relative ADC between tumor types were compared (Wilcoxon rank sum test, Fisher exact test). Histopathology and BRAF fusion/mutation status were reviewed. Associations of progression-free survival with diagnosis, imaging features, and BRAF status were examined by Cox proportional hazards models.
Pilocytic astrocytoma with gangliocytic differentiation appeared similar to pilocytic astrocytoma but had lower minimum relative ADC (mean, 1.01 ± 0.17 compared with 2.01 ± 0.38 for pilocytic astrocytoma; P = .0005) and was more commonly located within midline structures (P = .0034). BRAF status was similar for both groups. Non-total resection (hazard ratio, 52.64; P = .0002), pilocytic astrocytoma with gangliocytic differentiation diagnosis (hazard ratio, 4.66; P = .0104), and midline involvement (hazard ratio, 3.32; P = .0433) were associated with shorter progression-free survival.
Minimum relative ADC and tumor location may be useful adjuncts to histopathology in differentiating pilocytic astrocytoma with gangliocytic differentiation from pilocytic astrocytoma. Shorter progression-free survival in pilocytic astrocytoma with gangliocytic differentiation is likely due to a propensity for involvement of midline structures and poor resectability.
毛细胞型星形细胞瘤是儿童最常见的后颅窝肿瘤,其特征为KIAA1549 - BRAF融合,5年生存率极佳。具有神经节细胞分化的毛细胞型星形细胞瘤是一种最近定义的毛细胞型星形细胞瘤变体,包含类似于节细胞胶质瘤的神经胶质和神经元成分,可通过分子、放射学和组织病理学特征与经典节细胞胶质瘤相区分。本研究调查了影像学检查能否区分有或无神经节细胞分化的后颅窝毛细胞型星形细胞瘤。
对41例患有神经节细胞分化型毛细胞型星形细胞瘤(n = 7)或毛细胞型星形细胞瘤(n = 34)的儿童(年龄范围7个月至15岁;平均年龄7.3±3.7岁;58.5%为男性)的术前MRI(±CT)进行评估;比较肿瘤类型之间在肿瘤位置、形态以及最小相对表观扩散系数(ADC)方面的差异(Wilcoxon秩和检验、Fisher精确检验)。回顾组织病理学和BRAF融合/突变状态。通过Cox比例风险模型检查无进展生存期与诊断、影像学特征和BRAF状态之间的关联。
具有神经节细胞分化的毛细胞型星形细胞瘤外观与毛细胞型星形细胞瘤相似,但最小相对ADC较低(平均值为1.01±0.17,而毛细胞型星形细胞瘤为2.01±0.38;P = 0.0005),且更常见于中线结构内(P = 0.0034)。两组的BRAF状态相似。非全切(风险比,52.64;P = 0.0002)、神经节细胞分化型毛细胞型星形细胞瘤诊断(风险比,4.66;P = 0.0104)和中线受累(风险比,3.32;P = 0.0433)与较短的无进展生存期相关。
最小相对ADC和肿瘤位置可能是在组织病理学上区分神经节细胞分化型毛细胞型星形细胞瘤与毛细胞型星形细胞瘤的有用辅助手段。神经节细胞分化型毛细胞型星形细胞瘤无进展生存期较短可能是由于其倾向于累及中线结构且可切除性差。