Cheng T M, Coffey R J, Gelber B R, Scheithauer B W
Department of Neurologic Surgery, Mayo Clinic, Mayo Medical School, Rochester, Minnesota.
Neurosurgery. 1993 Jul;33(1):145-50. doi: 10.1227/00006123-199307000-00025.
Two young adult siblings independently developed similar neurological complaints that included headaches, photophobia, nausea, and intermittent lancinating facial pains. Magnetic resonance imaging revealed fourth ventricular lesions that required surgery in both patients. A pathological review revealed subependymomas with virtually identical histological features. The clinical features and common pathological findings of both patients suggest that familial subependymomas may have a maldevelopmental origin with genetic implications.
两名年轻成年兄妹独立出现了相似的神经系统症状,包括头痛、畏光、恶心和间歇性面部刺痛。磁共振成像显示两名患者均有第四脑室病变,需要进行手术。病理检查发现室管膜下瘤具有几乎相同的组织学特征。两名患者的临床特征和共同病理发现表明,家族性室管膜下瘤可能起源于发育异常,具有遗传意义。