Dimopoulos Vassilios G, Fountas Kostas N, Robinson Joe Sam
Department of Neurosurgery, Medical Center of Central Georgia, Mercer University, School of Medicine, Macon, Georgia, USA.
Neurosurg Focus. 2006 Jan 15;20(1):E8. doi: 10.3171/foc.2006.20.1.9.
Familial cases of intracranial ependymomas have been well documented in the literature. The authors present two cases from a family in which three members harbored intracranial ependymomas. A 54-year-old man with fourth ventricular ependymoma underwent resection of the tumor followed by radiation therapy. His son presented at age 36 years with a fourth ventricular tanycytic ependymoma and underwent total resection of the ependymoma with postoperative radiation therapy. The father's sister had been treated at another institution for a posterior fossa ependymoma.The association of ependymomas with molecular genetic alterations in chromosome 22 has been previously described. Further investigation of the genetic influences may lead to better therapeutic approaches for this relatively rare clinicopathological entity.
颅内室管膜瘤的家族性病例在文献中有充分记载。作者报告了来自一个家族的两例病例,该家族中有三名成员患有颅内室管膜瘤。一名患有第四脑室室管膜瘤的54岁男性接受了肿瘤切除术,随后进行了放射治疗。他的儿子在36岁时被诊断为第四脑室伸长细胞型室管膜瘤,并接受了室管膜瘤全切术及术后放射治疗。父亲的妹妹曾在另一机构接受后颅窝室管膜瘤治疗。此前已有文献描述室管膜瘤与22号染色体分子遗传改变之间的关联。对遗传影响的进一步研究可能会为这种相对罕见的临床病理实体带来更好的治疗方法。