Dağlioğlu Ergün, Cataltepe Oğuz, Akalan Nejat
Department of Neurosurgery, Hacettepe University Medical School, Ankara, Turkey.
Pediatr Neurosurg. 2003 May;38(5):223-31. doi: 10.1159/000069823.
Tumors involving the tectal region constitute a distinct subgroup of brain stem gliomas with an indolent clinical course. Here, we present the clinical and neuroradiologic features of 9 children with tectal tumors. All patients presented with signs and symptoms of hydrocephalus and were managed with ventriculoperitoneal shunt insertion. MRI studies revealed focal hyperintense lesions on T2-weighted images without any contrast enhancement, and no evidence of progression was demonstrated in any patient. We also reviewed the published series of tectal gliomas in the literature to compare with our results. Based on these and other published series, it was concluded that intrinsic tectal gliomas of childhood with sizes less than 2 cm in diameter and without any tumor extension or contrast enhancement constitute a specific subgroup of tectal masses which rarely display invasive clinical behavior and should be managed conservatively. CSF diversion procedures and long-term yearly follow-up examinations with MRI scans are sufficient in these patients.
累及顶盖区的肿瘤构成脑干胶质瘤的一个独特亚组,其临床病程较为缓慢。在此,我们呈现9例顶盖区肿瘤患儿的临床及神经放射学特征。所有患者均表现出脑积水的体征和症状,并接受了脑室腹腔分流术。MRI研究显示,T2加权图像上有局灶性高信号病变,无任何强化表现,且所有患者均未出现进展迹象。我们还回顾了文献中已发表的顶盖胶质瘤系列病例,以与我们的结果进行比较。基于这些及其他已发表的系列病例,得出的结论是,直径小于2厘米、无任何肿瘤扩展或强化表现的儿童原发性顶盖胶质瘤构成顶盖肿物的一个特定亚组,其很少表现出侵袭性临床行为,应采取保守治疗。对于这些患者,脑脊液分流手术及每年进行一次的长期MRI扫描随访检查就足够了。