MR Imaging Features to Differentiate Retinoblastoma from Coats' Disease and Persistent Fetal Vasculature.

Détails

Ressource 1Télécharger: 33266342_BIB_BEA453E2DEF7.pdf (9055.35 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_BEA453E2DEF7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
MR Imaging Features to Differentiate Retinoblastoma from Coats' Disease and Persistent Fetal Vasculature.
Périodique
Cancers
Auteur⸱e⸱s
Jansen R.W., de Bloeme C.M., Brisse H.J., Galluzzi P., Cardoen L., Göricke S., Maeder P., Cassoux N., Gauthier A., Schlueter S., Hadjistilianou T., Munier F.L., Castelijns J.A., van der Valk P., Moll A.C., de Jong M.C., de Graaf P.
ISSN
2072-6694 (Print)
ISSN-L
2072-6694
Statut éditorial
Publié
Date de publication
30/11/2020
Peer-reviewed
Oui
Volume
12
Numéro
12
Pages
E3592
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Résumé
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 (p < 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 (p < 0.001-0.022, specificity 91-100%). Additionally, three newly identified imaging features were exclusively present in pseudoretinoblastoma: intraretinal macrocysts (p < 0.001, 38% [9/24] in Coats' disease and 20% [2/10] in PFV), contrast enhancement outside the solid lesion (p < 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.
Mots-clé
Coats’ disease, MRI, persistent fetal vasculature, pseudoretinoblastoma, retinoblastoma
Pubmed
Web of science
Open Access
Oui
Création de la notice
21/12/2020 15:29
Dernière modification de la notice
08/08/2024 6:39
Données d'usage