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双侧视网膜母细胞瘤:对组织发生和治疗的见解

Trilateral retinoblastoma: insights into histogenesis and management.

作者信息

Marcus D M, Brooks S E, Leff G, McCormick R, Thompson T, Anfinson S, Lasudry J, Albert D M

机构信息

Department of Ophthalmology, Medical College of Georgia, Augusta 30912, USA.

出版信息

Surv Ophthalmol. 1998 Jul-Aug;43(1):59-70. doi: 10.1016/s0039-6257(98)00019-8.

Abstract

Trilateral retinoblastoma (TRb) is a syndrome involving midline intracranial malignancies in children with the heritable form of retinoblastoma. All cases of TRb reported from 1971 to 1997 were reviewed. The histopathologic findings, clinical features, treatment modalities, and survival rates from 80 cases were evaluated. Histopathologic findings from intracranial malignancies demonstrated primitive neuroectodermal tumors in 61.5% of cases. Various degrees of neuronal or photoreceptor differentiation were seen in the other 38.5% of cases. Autopsy, histopathologic, and radiologic examinations did not show a more definitive site of origin of these intracranial tumors, although "pinealoblastoma" was often the diagnosis reported. These findings, together with analysis of the histopathologic similarities among human primitive neuroectodermal tumors, pinealoblastoma, retinoblastoma, and ependymoblastoma, suggest that TRb more likely arises from a germinal layer of predisposed primitive subependymal neuroblasts that are not necessarily destined for pineal or photoreceptor differentiation. Trilateral tumors have also been found in transgenic mice expressing the simian virus 40 T-antigen. Transgenic murine intracranial tumors are primitive neuroectodermal tumors arising from the subependymal layer. Transgenic mice with the murine interphotoreceptor cell binding protein promoter and simian virus 40 T-antigen also develop pineal tumors. Trilateral retinoblastoma is usually fatal, with an average survival time of 11.2 months. Therapies include radiation, systemic chemotherapy, intrathecal chemotherapy, and surgical resection/craniotomy in combination with radiation and/or chemotherapy. Survival may be prolonged with combination chemotherapy (24.6 months) and if neuroradiologic screening identifies TRb before symptoms are present (23.5 months). Recent success with platinum-based chemoreduction of intraocular retinoblastoma may indicate a similar role for platinum-based chemotherapy in the treatment of TRb. Routine central nervous system imaging should be considered in the management of TRb.

摘要

双侧视网膜母细胞瘤(TRb)是一种综合征,涉及患有遗传性视网膜母细胞瘤的儿童中线颅内恶性肿瘤。回顾了1971年至1997年报告的所有TRb病例。评估了80例病例的组织病理学发现、临床特征、治疗方式和生存率。颅内恶性肿瘤的组织病理学发现显示,61.5%的病例为原始神经外胚层肿瘤。在另外38.5%的病例中可见不同程度的神经元或光感受器分化。尸检、组织病理学和放射学检查均未显示这些颅内肿瘤更明确的起源部位,尽管报告的诊断通常为“松果体母细胞瘤”。这些发现,连同对人类原始神经外胚层肿瘤、松果体母细胞瘤、视网膜母细胞瘤和室管膜母细胞瘤之间组织病理学相似性的分析,表明TRb更可能起源于易患的原始室管膜下神经母细胞的生发层,这些神经母细胞不一定注定要分化为松果体或光感受器。在表达猿猴病毒40 T抗原的转基因小鼠中也发现了双侧肿瘤。转基因小鼠颅内肿瘤是起源于室管膜下层的原始神经外胚层肿瘤。具有鼠类光感受器间细胞结合蛋白启动子和猿猴病毒40 T抗原的转基因小鼠也会发生松果体肿瘤。双侧视网膜母细胞瘤通常是致命的,平均生存时间为11.2个月。治疗方法包括放疗、全身化疗、鞘内化疗以及手术切除/开颅术联合放疗和/或化疗。联合化疗(24.6个月)以及如果神经放射学筛查在出现症状之前识别出TRb(23.5个月),生存时间可能会延长。基于铂的眼内视网膜母细胞瘤化疗减积术最近取得的成功可能表明基于铂的化疗在TRb治疗中具有类似作用。在TRb的管理中应考虑进行常规中枢神经系统成像检查。

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