Jansen Robin W, de Bloeme Christiaan M, Brisse Hervé J, Galluzzi Paolo, Cardoen Liesbeth, Göricke Sophia, Maeder Philippe, Cassoux Nathalie, Gauthier Arnaud, Schlueter Sabrina, Hadjistilianou Theodora, Munier Francis L, Castelijns Jonas A, van der Valk Paul, Moll Annette C, de Jong Marcus C, de Graaf Pim
Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Universiteit Amsterdam, Cancer Center Amsterdam, 1081HV Amsterdam, The Netherlands.
Department of Radiology, Institut Curie, Paris University, 75005 Paris, France.
Cancers (Basel). 2020 Nov 30;12(12):3592. doi: 10.3390/cancers12123592.
Retinoblastoma mimickers, or pseudoretinoblastoma, are conditions that show similarities with the pediatric cancer retinoblastoma. However, false-positive retinoblastoma diagnosis can cause mistreatment, while false-negative diagnosis can cause life-threatening treatment delay. The purpose of this study is to identify the MR imaging features that best differentiate between retinoblastoma and the most common pseudoretinoblastoma diagnoses: Coats' disease and persistent fetal vasculature (PFV). Here, six expert radiologists performed retrospective assessments (blinded for diagnosis) of MR images of patients with a final diagnosis based on histopathology or clinical follow-up. Associations between 20 predefined imaging features and diagnosis were assessed with exact tests corrected for multiple hypothesis testing. Sixty-six patients were included, of which 33 (50%) were retinoblastoma and 33 (50%) pseudoretinoblastoma patients. A larger eye size, vitreous seeding, and sharp-V-shaped retinal detachment were almost exclusively found in retinoblastoma ( < 0.001-0.022, specificity 93-97%). Features that were almost exclusively found in pseudoretinoblastoma included smaller eye size, ciliary/lens deformations, optic nerve atrophy, a central stalk between optic disc and lens, Y-shaped retinal detachment, and absence of calcifications ( < 0.001-0.022, specificity 91-100%). Additionally, three newly identified imaging features were exclusively present in pseudoretinoblastoma: intraretinal macrocysts ( < 0.001, 38% [9/24] in Coats' disease and 20% [2/10] in PFV), contrast enhancement outside the solid lesion ( < 0.001, 30% [7/23] in Coats' disease and 57% [4/7] in PFV), and enhancing subfoveal nodules (38% [9/24] in Coats' disease). An assessment strategy was proposed for MR imaging differentiation between retinoblastoma and pseudoretinoblastoma, including three newly identified differentiating MR imaging features.
视网膜母细胞瘤模仿者,或假性视网膜母细胞瘤,是与儿童癌症视网膜母细胞瘤表现出相似性的病症。然而,视网膜母细胞瘤的假阳性诊断会导致不当治疗,而假阴性诊断会导致危及生命的治疗延迟。本研究的目的是确定最能区分视网膜母细胞瘤与最常见的假性视网膜母细胞瘤诊断(科茨病和永存原始玻璃体增生症(PFV))的磁共振成像(MR)特征。在此,六位放射学专家对根据组织病理学或临床随访得出最终诊断的患者的MR图像进行了回顾性评估(诊断结果保密)。通过针对多重假设检验校正的精确检验评估了20个预定义成像特征与诊断之间的关联。纳入了66例患者,其中33例(50%)为视网膜母细胞瘤患者,33例(50%)为假性视网膜母细胞瘤患者。更大的眼球大小、玻璃体播散和尖锐的V形视网膜脱离几乎仅见于视网膜母细胞瘤(<0.001 - 0.022,特异性93 - 97%)。几乎仅见于假性视网膜母细胞瘤的特征包括较小的眼球大小、睫状体/晶状体变形、视神经萎缩、视盘与晶状体之间的中央柄、Y形视网膜脱离以及无钙化(<0.001 - 0.022,特异性91 - 100%)。此外,三个新发现的成像特征仅见于假性视网膜母细胞瘤:视网膜内大囊肿(<0.001,科茨病中为38%[9/24],PFV中为20%[2/10])、实性病变外的对比增强(<0.001,科茨病中为30%[7/23],PFV中为57%[4/7])以及黄斑下强化结节(科茨病中为38%[9/24])。提出了一种用于视网膜母细胞瘤与假性视网膜母细胞瘤之间MR成像鉴别的评估策略,包括三个新发现的鉴别性MR成像特征。