Abstract | PURPOSE: METHODS: This is an interventional case report. A boy with a paternal history of retinoblastoma and in utero identification of an RB1 mutation was monitored beginning at 2 weeks of age. When the patient was 6 months old, the first tumor was detected and treatment with a direct, ablative, large spot-size diode laser was initiated. During a 38-month period of follow-up, the patient received 23 laser treatments and 3 periocular carboplatin injections (20 mg in 2 mL) to treat 3 tumors in 1 eye. RESULTS: Initially, diode laser ablation of the tumors produced a favorable involutional response of the tumors, associated with a decrease in size and vascularity. Despite aggressive treatment with 12 consecutive laser treatments for 9.7 months, progressive tumor growth was observed in the superonasal tumor, whereas the other 2 tumors remained quiescent. At that time, a series of three focal periocular injections of carboplatin were administered in combination with continued laser ablation. The tumor regressed with type 4 chorioretinal scarring. No systemic chemotherapy or radiation was required. CONCLUSION:
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Authors | Theodore Leng, Colleen M Cebulla, Amy C Schefler, Timothy G Murray |
Journal | Retina (Philadelphia, Pa.)
(Retina)
Vol. 30
Issue 4 Suppl
Pg. S66-8
(Apr 2010)
ISSN: 1539-2864 [Electronic] United States |
PMID | 20419851
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Antineoplastic Agents
- Retinoblastoma Protein
- Carboplatin
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Topics |
- Antineoplastic Agents
(therapeutic use)
- Carboplatin
(therapeutic use)
- Combined Modality Therapy
- Humans
- Infant, Newborn
- Injections
- Laser Coagulation
- Lasers, Semiconductor
(therapeutic use)
- Male
- Mutation
- Retinal Neoplasms
(drug therapy, genetics, surgery, therapy)
- Retinoblastoma
(drug therapy, genetics, surgery, therapy)
- Retinoblastoma Protein
(genetics)
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