Article ID Journal Published Year Pages File Type
4029947 Ophthalmology 2007 7 Pages PDF
Abstract
New tumors continue to form in patients with hereditary retinoblastoma despite treatment with primary systemic chemotherapy. Younger patients and those with a positive family history are more likely to have new tumors formed. However, chemotherapy may impact small previously undetected lesions by slowing their growth and facilitating later focal consolidation.
Related Topics
Health Sciences Medicine and Dentistry Ophthalmology
Authors
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