Department of Neurosurgery, The Newcastle Upon Tyne Hospitals, Newcastle, United Kingdom.
Neurosurgery. 2011 May;68(5):1293-8; discussion 1298-9. doi: 10.1227/NEU.0b013e31820b522a.
Recent studies suggest a possible origin of human gliomas from subventricular zone (SVZ) stem cells.
To evaluate the relationship of World Health Organization grade II gliomas (GIIGs) with the SVZ and to investigate the presence of different genetic patterns, depending on their relationship with the SVZ.
Forty-three consecutive patients were operated on for GIIG. Preoperative fluid-attenuated inversion recovery-weighted magnetic resonance images were reviewed to assess the presence of cortical involvement and the relationship between gliomas and the SVZ. Patients were divided into 2 groups: group 1, tumors in contact with the SVZ; and group 2, tumors not in contact with the SVZ. Preoperative and postoperative tumor volumes were calculated. Genetic analysis was performed to study 1p19q allelic loss.
Twenty-four patients were in group 1 and 19 in group 2. All tumors were in contact with the cortex. Preoperative volume was significantly larger in group 1 than in group 2 (P = .003). The proportion of total and subtotal resections was higher in group 2 (P = .01). Insular tumors never showed 1p19q codeletions. Noninsular tumors exhibited a significantly different incidence of complete 1p19q codeletion, with allelic loss more common in group 1 (P = .03).
GIIGs showed a constant relationship with the cortex and a larger volume when they came in contact with the ventricles. A distinct genetic pattern was found in noninsular SVZ GIIGs. This parameter can be considered for therapeutic management.
最近的研究表明,人类脑胶质瘤可能起源于侧脑室下区(SVZ)干细胞。
评估世界卫生组织二级胶质瘤(GIIG)与 SVZ 的关系,并研究不同遗传模式的存在,取决于它们与 SVZ 的关系。
对 43 例连续接受 GIIG 手术的患者进行研究。回顾术前液体衰减反转恢复加权磁共振成像,以评估皮质受累情况以及胶质瘤与 SVZ 的关系。将患者分为两组:组 1,肿瘤与 SVZ 接触;组 2,肿瘤不与 SVZ 接触。计算术前和术后肿瘤体积。进行遗传分析以研究 1p19q 等位基因缺失。
24 例患者为组 1,19 例患者为组 2。所有肿瘤均与皮质接触。组 1 的术前体积明显大于组 2(P =.003)。组 2 中完全和次全切除术的比例较高(P =.01)。岛叶肿瘤从不出现 1p19q 联合缺失。非岛叶肿瘤的完全 1p19q 联合缺失发生率明显不同,组 1 的等位基因缺失更为常见(P =.03)。
GIIG 与皮质始终存在联系,当与脑室接触时体积更大。非岛叶 SVZ GIIG 存在明显不同的遗传模式。该参数可考虑用于治疗管理。