Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4029947 | Ophthalmology | 2007 | 7 Pages |
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.
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Authors
Matthew W. MD, FACS, Barrett G. MD, FACS, Catherine A. MS, Carlos MD,