Retinoblastoma: What the Neuroradiologist Needs to Know

被引:22
|
作者
Silvera, V. M. [1 ]
Guerin, J. B. [1 ]
Brinjikji, W. [1 ,2 ]
Dalvin, L. A. [3 ]
机构
[1] Mayo Clin, Dept Neuroradiol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Neurosurg, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Ophthalmol, 200 1st St SW, Rochester, MN 55905 USA
关键词
OPTIC-NERVE INVASION; PRIMARY INTRAARTERIAL CHEMOTHERAPY; INTERNATIONAL-CLASSIFICATION; RISK-FACTORS; NEOADJUVANT CHEMOTHERAPY; HISTOPATHOLOGIC FINDINGS; SURFACE COILS; MRI; EYES; CHEMOREDUCTION;
D O I
10.3174/ajnr.A6949
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Retinoblastoma is the most common primary intraocular tumor of childhood. Accurate diagnosis at an early stage is important to maximize patient survival, globe salvage, and visual acuity. Management of retinoblastoma is individualized based on the presenting clinical and imaging features of the tumor, and a multidisciplinary team is required to optimize patient outcomes. The neuroradiologist is a key member of the retinoblastoma care team and should be familiar with characteristic diagnostic and prognostic imaging features of this disease. Furthermore, with the adoption of intra-arterial chemotherapy as a standard of care option for globe salvage therapy in many centers, the interventional neuroradiologist may play an active role in retinoblastoma treatment. In this review, we discuss the clinical presentation of retinoblastoma, ophthalmic imaging modalities, neuroradiology imaging features, and current treatment options.
引用
收藏
页码:618 / 626
页数:9
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