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High-risk retinoblastoma based on international classification of retinoblastoma: analysis of 519 enucleated eyes.基于国际视网膜母细胞瘤分类的高危视网膜母细胞瘤:519 例眼球摘除眼分析。
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视网膜母细胞瘤中的视神经遮挡:视神经侵犯的一个危险因素?

Optic Nerve Obscuration in Retinoblastoma: A Risk Factor for Optic Nerve Invasion?

作者信息

Berry Jesse L, Zolfaghari Emily, Chen Alexander, Murphree A Linn, Jubran Rima, Kim Jonathan W

机构信息

USC Roski Eye Institute, Keck Medical School of the University of Southern California, California, USA.

The Vision Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Los Angeles, California, USA.

出版信息

Ocul Oncol Pathol. 2017 Nov;3(4):283-291. doi: 10.1159/000464468. Epub 2017 Apr 7.

DOI:10.1159/000464468
PMID:29344482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5757559/
Abstract

BACKGROUND

The objective of this study is to evaluate the risk of optic nerve invasion associated with optic nerve obscuration at diagnosis or persisting during treatment.

METHODS

Retrospective review from 2011-2016 of patients with advanced retinoblastoma (Group D/E) with complete obscuration of the nerve at diagnosis and a second group of patients with persistent, complete obscuration throughout treatment.

RESULTS

Advanced retinoblastoma was diagnosed in 102 eyes of 86 patients. The optic nerve was obscured in 69 eyes (68%) at diagnosis. Of these, 30 (43%) underwent salvage therapy and 39 (57%) primary enucleation. Histopathologic analysis of primarily enucleated eyes showed 41% prelaminar and 15% postlaminar invasion. Four eyes in the salvage group demonstrated persistent nerve obscuration; 2 were subsequently enucleated without evidence of nerve invasion. Average follow-up was 23.5 months (range 1-62 months).

CONCLUSIONS AND RELEVANCE

Optic nerve obscuration at diagnosis may be associated with postlaminar optic nerve invasion. While persistent, complete obscuration of the optic nerve by retinoblastoma during treatment is a poor prognostic sign for both globe salvage and vision, it does not appear, in this small cohort, to increase the risk of optic nerve invasion. With appropriate control of the intraocular tumor, these eyes can be salvaged.

摘要

背景

本研究的目的是评估诊断时或治疗期间持续存在的视神经遮挡与视神经侵犯风险之间的关系。

方法

回顾性分析2011年至2016年期间诊断时视神经完全遮挡的晚期视网膜母细胞瘤患者(D/E组),以及另一组在整个治疗过程中视神经持续完全遮挡的患者。

结果

86例患者的102只眼中诊断为晚期视网膜母细胞瘤。诊断时69只眼(68%)视神经被遮挡。其中,30只眼(43%)接受了挽救性治疗,39只眼(57%)接受了一期眼球摘除术。一期眼球摘除术眼的组织病理学分析显示,41%为筛板前侵犯,15%为筛板后侵犯。挽救组中有4只眼视神经持续遮挡;2只眼随后接受了眼球摘除术,未发现神经侵犯证据。平均随访时间为23.5个月(范围1至62个月)。

结论及意义

诊断时视神经遮挡可能与筛板后视神经侵犯有关。虽然视网膜母细胞瘤在治疗期间持续、完全遮挡视神经对眼球挽救和视力来说都是不良预后征象,但在这个小队列中,它似乎并未增加视神经侵犯的风险。通过适当控制眼内肿瘤,这些眼可以得到挽救。