2017, Number 1
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Rev Med MD 2017; 8.9 (1)
Cavitary Retinoblastoma: A Case Report
González-Pérez G, Robles-Yeme D, Muñoz-Solórzano B
Language: Spanish
References: 13
Page: 77-80
PDF size: 731.00 Kb.
ABSTRACT
Retinoblastoma is a potentially fatal malignant intraocular neoplasm, occurring predominantly during infancy.
Rarely, it manifests with ophthalmoscopically visible cavities inside the tumor, describing it as cavitary retinoblastoma,
which presents chemoresistence and radioresistance, as well as a more favorable prognosis in most cases. We present a
clinical case with a diagnosis of cavitary retinoblastoma and its presentation as well as response to treatment. More
studies and guides are needed to focus the approach and relapse rates.
REFERENCES
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10.Fabian I, Naeem Z, et al. Longterm visual acuity, strabismus and nystagmus outcomes following multimodality treatment in group D Retinoblastoma eyes. Am J Ophthalmol. 2017.
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