双侧视网膜母细胞瘤患者的MRI筛查。

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY Seminars in Ophthalmology Pub Date : 2025-01-08 DOI:10.1080/08820538.2025.2450681
Ronald Hershcovici, Shahar Frenkel, Gal Goldstein, Jacob Pe'er, Maya Eiger-Moscovich
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引用次数: 0

摘要

目的:三边视网膜母细胞瘤(TRB)是遗传性视网膜母细胞瘤患者的颅内肿瘤,是一种非常罕见的致命性疾病。许多眼科肿瘤中心通过脑成像对视网膜母细胞瘤患者进行常规筛查。然而,关于其延长TRB患者生存的能力和需要治疗的数量存在争议。我们建议对双侧视网膜母细胞瘤患者进行基线筛查脑成像,然后根据临床需要进行影像学检查。我们的目标是看看这个筛查计划是否对患者的生存有影响。方法:回顾性观察1986年7月1日至2020年2月1日在某三级医疗中心眼科肿瘤科诊断为双侧视网膜母细胞瘤的患者,随访至少36个月或视网膜母细胞瘤相关死亡。我们收集了患者的人口统计学、临床特征、系统评估、治疗、随访和结果的数据。结果:本研究纳入109例双侧视网膜母细胞瘤患者,其中男性60例,女性49例,中位年龄7.0个月(范围0.43-70.5个月)。生殖系突变43例(39.4%),体细胞突变15例(13.8%)。51例(46.8%)患者未记录遗传状况。58例患者(53.0%)接受了基线脑成像(42例MRI和16例CT扫描),所有患者均在正常范围内。在中位随访138个月(范围19-787个月)期间,35名儿童进行了随访脑成像(25例MRI, 10例CT)。1例患者在随访期间出现症状性TRB,存活且无病(0.9%,Cl:0.02%-5.6%)。观察生存期,6名患者(5.5%)发展为转移性疾病,8名患者(7.3%)死亡,所有死亡均与视网膜母细胞瘤相关。结论:由于TRB罕见,常规脑MRI基线筛查可能足够,避免麻醉、费用、痛苦和不必要的干预,对患者的生存无显著影响。然而,由于TRB的致死率和治疗发病率,在3岁之前定期进行脑MRI是一个合理的选择。
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Brain MRI Screening for Bilateral Retinoblastoma Patients.

Purpose: Trilateral retinoblastoma (TRB), intracranial neoplasm in heritable retinoblastoma patients, is a very rare fatal disease. Many ocular oncology centers conduct routine screening of retinoblastoma patients by brain imaging. Nevertheless, there is a debate regarding its ability to prolong TRB patients' survival and the number-needed-to-treat. We recommend baseline screening brain imaging in bilateral retinoblastoma patients, followed by imaging according to clinical need. We aim to see if this screening schedule has an impact on patients' survival.

Methods: In a retrospective observational study, we reviewed the medical records of patients diagnosed with bilateral retinoblastoma at a tertiary medical center ocular oncology unit between 1.7.1986 and 1.2.2020, who had at least 36 months follow-up or retinoblastoma-related death. We collected data on patients' demographics, clinical features, systemic evaluation, treatment, follow-up, and outcome.

Results: The analysis included 109 patients, 60 males and 49 females, diagnosed with bilateral retinoblastoma at a median age of 7.0 months (range 0.43-70.5 months). Germline mutation was found in 43 patients (39.4%) and somatic mutation in 15 patients (13.8%). Genetic status was not recorded in 51 patients (46.8%). Fifty-eight patients (53.0%) underwent baseline brain imaging (MRI in 42 patients and CT scan in 16 patients), in all of whom it was within normal limits. During a median follow-up of 138 months (range 19-787 months), 35 children had follow-up brain imaging (MRI in 25 patients and CT in 10 patients). One patient developed symptomatic TRB during follow-up, and is alive and disease-free (0.9%, Cl:0.02%-5.6%). Looking at survival, six patients (5.5%) developed metastatic disease, and eight patients (7.3%) expired, in all of whom death was retinoblastoma-related.

Conclusions: Due to TRB rarity, routine screening by baseline brain MRI may be sufficient, avoiding anesthesia, expenses, distress, and unnecessary interventions, without a significant impact on patients' survival. Nevertheless, due to TRB fatality and treatment morbidity, periodic brain MRI until age 3 is a legitimate option.

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来源期刊
Seminars in Ophthalmology
Seminars in Ophthalmology OPHTHALMOLOGY-
CiteScore
3.20
自引率
0.00%
发文量
80
审稿时长
>12 weeks
期刊介绍: Seminars in Ophthalmology offers current, clinically oriented reviews on the diagnosis and treatment of ophthalmic disorders. Each issue focuses on a single topic, with a primary emphasis on appropriate surgical techniques.
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