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Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up

PURPOSE: To evaluate the safety and efficacy of intravitreal injections of bevacizumab (Avastin(®)) as a treatment option for radiation maculopathy secondary to proton beam radiotherapy for choroidal melanoma. CASE: A 61-year-old woman presented with a gradual decrease in left eye visual acuity (VA)...

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Autores principales: Loukianou, Eleni, Brouzas, Dimitrios, Georgopoulou, Eleni, Koutsandrea, Chrysanthi, Apostolopoulos, Michael
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878959/
https://www.ncbi.nlm.nih.gov/pubmed/20526443
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author Loukianou, Eleni
Brouzas, Dimitrios
Georgopoulou, Eleni
Koutsandrea, Chrysanthi
Apostolopoulos, Michael
author_facet Loukianou, Eleni
Brouzas, Dimitrios
Georgopoulou, Eleni
Koutsandrea, Chrysanthi
Apostolopoulos, Michael
author_sort Loukianou, Eleni
collection PubMed
description PURPOSE: To evaluate the safety and efficacy of intravitreal injections of bevacizumab (Avastin(®)) as a treatment option for radiation maculopathy secondary to proton beam radiotherapy for choroidal melanoma. CASE: A 61-year-old woman presented with a gradual decrease in left eye visual acuity (VA) 29 months after proton beam radiotherapy for choroidal melanoma. On presentation, her best-corrected VA (BCVA) was 2/10 in the left eye and the intraocular pressure was 15 mmHg. Fundoscopy revealed cystoid macular edema, intraretinal hemorrhages, epiretinal membrane in the posterior pole, and residual tumor scar with exudative retinal detachment and hard exudates in the periphery of the superotemporal quadrant. A treatment with intravitreal injections of bevacizumab (Avastin(®)) was recommended. The injections were performed on a six-weekly basis. RESULTS: The central retinal thickness prior to the treatment was 458 μm. After the first intravitreal injection of bevacizumab, the retinal thickness at the centre of the fovea was reduced to 322 μm. After the third injection, the central retinal thickness was 359 μm and 18 months after presentation, it reduced to 334 μm. The BCVA increased to 3/10 after the intravitreal injections of bevacizumab and remained stable during the follow-up period. The intraocular pressure was within normal range during the follow-up period. CONCLUSION: Bevacizumab should be regarded as a treatment option for macular edema due to proton beam radiotherapy for choroidal melanoma. By reducing the central retinal thickness, intravitreal bevacizumab can improve VA or ameliorate further decline caused by radiation maculopathy.
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spelling pubmed-28789592010-06-04 Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up Loukianou, Eleni Brouzas, Dimitrios Georgopoulou, Eleni Koutsandrea, Chrysanthi Apostolopoulos, Michael Ther Clin Risk Manag Case Report PURPOSE: To evaluate the safety and efficacy of intravitreal injections of bevacizumab (Avastin(®)) as a treatment option for radiation maculopathy secondary to proton beam radiotherapy for choroidal melanoma. CASE: A 61-year-old woman presented with a gradual decrease in left eye visual acuity (VA) 29 months after proton beam radiotherapy for choroidal melanoma. On presentation, her best-corrected VA (BCVA) was 2/10 in the left eye and the intraocular pressure was 15 mmHg. Fundoscopy revealed cystoid macular edema, intraretinal hemorrhages, epiretinal membrane in the posterior pole, and residual tumor scar with exudative retinal detachment and hard exudates in the periphery of the superotemporal quadrant. A treatment with intravitreal injections of bevacizumab (Avastin(®)) was recommended. The injections were performed on a six-weekly basis. RESULTS: The central retinal thickness prior to the treatment was 458 μm. After the first intravitreal injection of bevacizumab, the retinal thickness at the centre of the fovea was reduced to 322 μm. After the third injection, the central retinal thickness was 359 μm and 18 months after presentation, it reduced to 334 μm. The BCVA increased to 3/10 after the intravitreal injections of bevacizumab and remained stable during the follow-up period. The intraocular pressure was within normal range during the follow-up period. CONCLUSION: Bevacizumab should be regarded as a treatment option for macular edema due to proton beam radiotherapy for choroidal melanoma. By reducing the central retinal thickness, intravitreal bevacizumab can improve VA or ameliorate further decline caused by radiation maculopathy. Dove Medical Press 2010 2010-05-25 /pmc/articles/PMC2878959/ /pubmed/20526443 Text en © 2010 Loukianou et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Case Report
Loukianou, Eleni
Brouzas, Dimitrios
Georgopoulou, Eleni
Koutsandrea, Chrysanthi
Apostolopoulos, Michael
Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up
title Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up
title_full Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up
title_fullStr Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up
title_full_unstemmed Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up
title_short Intravitreal bevacizumab for macular edema due to proton beam radiotherapy: Favorable results shown after eighteen months follow-up
title_sort intravitreal bevacizumab for macular edema due to proton beam radiotherapy: favorable results shown after eighteen months follow-up
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878959/
https://www.ncbi.nlm.nih.gov/pubmed/20526443
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