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报告１例ｖｏｎＨｉｐｐｅｌ－Ｌｉｎｄａｕ病伴双眼眼内骨化的病例。该女性患者除有多灶性的视网膜血管瘤及严重的晚期并发症外，其中枢神经系统的毛细血管母细胞启发生于额叶实属罕见。既往病史及ＣＴ检查有助于限内骨化的诊断。
One case of von Hippel-Lindau disease with binocular ossification was reported. In addition to multifocal retinal hemangiomas and severe late complications, this female patient has rare central nervous system capillarity derived from the frontal lobe. Past medical history and CT examination can help limit the diagnosis of ossification.