首页> 外文期刊>Journal of pediatric ophthalmology and strabismus >Hand-held spectral-domain optical coherence tomography of small macular retinoblastoma in infants before and after chemotherapy
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Hand-held spectral-domain optical coherence tomography of small macular retinoblastoma in infants before and after chemotherapy

机译:婴儿小黄斑视网膜母细胞瘤化疗前后的手持式光谱域光学相干断层扫描

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Purpose: To demonstrate the utility of hand-held spectral-domain optical coherence tomography (SD-OCT) in assessing retinal structure in cases of macular retinoblastoma. Methods: In this retrospective, observational case series, three young children with macular retinoblastoma were treated at a tertiary care hospital. At examination under anesthesia, each patient was evaluated with SD-OCT for analysis of retinal tumor and macula. The main outcomes were retinal morphology before and after chemotherapy. Results: The mean patient age was 16 months (median: 9 months; range: 7 to 33 months). All patients had small exophytic macular retinoblastoma with subretinal fluid in the foveola. At presentation, the mean tumor thickness was 4.8 mm (range: 4.0 to 6.0 mm) and mean tumor base was 10.3 mm (range: 8.0 to 12.0 mm). SD-OCT documented tumor surface as smooth (n = 2) or irregular (n = 1), involvement of full-thickness retina (n = 3), and optical density as low (n = 3). The surrounding retina showed abrupt transition to tumor (n = 3), without intraretinal edema (n = 3), and with underlying subretinal fluid (n = 3). Following chemotherapy, all tumors showed regression with mean thickness of 2.6 mm (range: 2.2 to 3.0 mm). SD-OCT documented tumor surface as smooth (n = 1) or irregular (n = 2), and optical density as medium (n = 1) or high (n = 2). At the tumor site, the retina showed full-thickness disorganization but with abrupt transition to normal retina (n = 3). The foveola was anatomically intact (n = 1) or with outer retinal thinning (n = 2). Subretinal fluid was resolved in each case (n = 3). Conclusions: SD-OCT can provide precise anatomic monitoring of the macular region in infants and young children with small macular retinoblastoma. This may serve as a guide for visual potential in the preverbal child.
机译:目的:演示手持光谱域光学相干断层扫描(SD-OCT)在评估黄斑视网膜母细胞瘤视网膜结构中的实用性。方法:在此回顾性观察病例系列中,三级黄斑视网膜母细胞瘤患儿在三级医院接受了治疗。在麻醉下检查时,每位患者均接受SD-OCT评估,以分析视网膜肿瘤和黄斑。主要结局是化疗前后的视网膜形态。结果:患者平均年龄为16个月(中位数:9个月;范围:7至33个月)。所有患者均患有小眼外生性黄斑视网膜母细胞瘤,黄斑中心带视网膜下液。在介绍时,平均肿瘤厚度为4.8毫米(范围:4.0至6.0毫米),平均肿瘤基底为10.3毫米(范围:8.0至12.0毫米)。 SD-OCT记录的肿瘤表面光滑(n = 2)或不规则(n = 1),累及全层视网膜(n = 3),光密度低(n = 3)。周围的视网膜显示突然过渡到肿瘤(n = 3),无视网膜内水肿(n = 3),并且具有潜在的视网膜下液(n = 3)。化疗后,所有肿瘤均出现退缩,平均厚度为2.6 mm(范围:2.2至3.0 mm)。 SD-OCT记录的肿瘤表面光滑(n = 1)或不规则(n = 2),光密度中等(n = 1)或高(n = 2)。在肿瘤部位,视网膜表现出全层杂乱无章,但突然过渡到正常视网膜(n = 3)。中心凹在解剖学上是完整的(n = 1)或视网膜外变薄(n = 2)。在每种情况下,视网膜下液均得到解决(n = 3)。结论:SD-OCT可以为小黄斑视网膜母细胞瘤的婴幼儿的黄斑区域提供精确的解剖学监测。这可以作为前言儿童视觉潜能的指导。

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