Nelson S C, Friedman H S, Oakes W J, Halperin E C, Tien R, Fuller G N, Hockenberger B, Scroggs M W, Moncino M, Kurtzberg J
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710.
Am J Ophthalmol. 1992 Jul 15;114(1):23-9. doi: 10.1016/s0002-9394(14)77408-2.
Trilateral retinoblastoma, the intracranial malignancy associated with bilateral retinoblastoma, is an uncommon and clinically aggressive malignancy with a uniformly fatal outcome. Three children with newly diagnosed trilateral retinoblastoma were treated with systemic (cyclophosphamide and vincristine) and intrathecal (methotrexate, hydrocortisone, and cytarabine) chemotherapy, as well as craniospinal irradiation (one patient) in addition to therapy of the eye lesions. All three patients have had partial or complete response of the pineal tumors to chemotherapy, with no active disease eight or more years, 33 or more months, and 12 or more months, respectively, after diagnosis of the lesions.
三侧性视网膜母细胞瘤是一种与双侧视网膜母细胞瘤相关的颅内恶性肿瘤,是一种罕见且具有临床侵袭性的恶性肿瘤,预后通常是致命的。三名新诊断为三侧性视网膜母细胞瘤的儿童接受了全身化疗(环磷酰胺和长春新碱)和鞘内化疗(甲氨蝶呤、氢化可的松和阿糖胞苷),除了眼部病变的治疗外,其中一名患者还接受了全脑全脊髓放疗。所有三名患者的松果体肿瘤对化疗均有部分或完全反应,分别在病变诊断后八年或更长时间、33个月或更长时间以及12个月或更长时间无活动性疾病。