Volume 31, Issue 3 pp. 446-458
Views and Reviews

Neuroimaging in Children with Ophthalmological Complaints: A Review

Mika Shapira Rootman

Corresponding Author

Mika Shapira Rootman

Department of Radiology, Schneider Children's Medical Center of Israel, Petah Tikva, Israel

Sackler Faculty of Medicine, Tel-Aviv University

Correspondence: Address correspondence to Mika Shapira Rootman, Department of Radiology, Schneider Children's Medical center of Israel, 14 Kaplan Street, PO Box 559, Petach Tikva 4920235, Israel. E-mail: [email protected].

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Gad Dotan

Gad Dotan

Ophthalmology Unit, Schneider Children's Medical center of Israel, Petac Tikva, Israel

Sackler Faculty of Medicine, Tel-Aviv University

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Osnat Konen

Osnat Konen

Department of Radiology, Schneider Children's Medical Center of Israel, Petah Tikva, Israel

Sackler Faculty of Medicine, Tel-Aviv University

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First published: 22 February 2021
Citations: 2

Acknowledgments and Disclosure: The authors received no specific funding for this work. There is no potential financial conflict and nothing to disclose.

We would like to thank Prof. Liora Korenreich for her assistance and support.

ABSTRACT

Pediatric patients are commonly referred to imaging following abnormal ophthalmological examinations. Common indications include papilledema, altered vision, strabismus, nystagmus, anisocoria, proptosis, coloboma, and leukocoria. Magnetic resonance imaging (MRI) of the brain and orbits (with or without contrast material administration) is typically the imaging modality of choice. However, a cranial CT scan is sometimes initially performed, particularly when MRI is not readily available. Familiarity with the various ophthalmological conditions may assist the radiologist in formulating differential diagnoses and proper MRI protocols afterward. Although MRI of the brain and orbits usually suffices, further refinements are sometimes warranted to enable suitable assessment and accurate diagnosis. For example, the assessment of children with sudden onset anisocoria associated with Horner syndrome will require imaging of the entire oculosympathetic pathway, including the brain, orbits, neck, and chest. Dedicated orbital scans should cover the area between the hard palate and approximately 1 cm above the orbits in the axial plane and extend from the lens to the midpons in the coronal plane. Fat-suppressed T2-weighted fast spin echo sequences should enable proper assessment of the globes, optic nerves, and perioptic subarachnoid spaces. Contrast material should be given judiciously, ideally according to clinical circumstances and precontrast scans. In this review, we discuss the major indications for imaging following abnormal ophthalmological examinations.

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