Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections

Detalhes bibliográficos
Autor(a) principal: Couceiro, Rita
Data de Publicação: 2018
Outros Autores: Amaro, Miguel, Ferreira, Ana, Cavalheiro, Diogo
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.48560/rspo.13416
Resumo: Purpose: to report a case of idiopathic choroidal neovascularization (CNV) in a pediatric patient successfully treated with intravitreal bevacizumab injections.  Methods: case report of a 10 year-old patient, who presented with reduced unilateral visual acuity during a visual screening. Complete ophthalmological examination was performed, along with fluorescein angiography, spectral domain optic coherence tomography (SD-OCT), fundus autofluorescence, ocular ultrasound, magnetic resonance imaging (MRI) of the brain and orbits and infectious serologies. Results: visual acuity was 20/400 in the left eye (OS) and 20/20 in the right eye (OD). No significant refractive error was detected. Fundoscopy in OS revealed a subretinal macular lesion associated with subretinal hemorrhage and fluid. Fluorescein angiography and SD-OCT confirmed the presence of NVC. Retinal hereditary dystrophies, along with infectious and neoplastic causes were excluded. The patient underwent two intravitreal bevacizumab injections in OS with a 3 months interval. Treatment resulted in progressive fibrosis of NVC, resolution of subretinal fluid and improvement of visual acuity in OS to 20/125, which remained stable 4 years after treatment. Conclusions: In the case of pediatric NVC, retinal hereditary dystrophies along with infectious and neoplastic causes should be excluded after a thorough investigation. No standard treatment for CNV in children has yet been validated. In our patient anti-vascular endothelial growth factor (VEGF) treatment induced regression of the CNV and resolution of subretinal fluid with a modest recovery in visual acuity and no reported ocular or systemic side effects. 
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spelling Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injectionsComunicações Curtas e Imagens em OftalmologiaPurpose: to report a case of idiopathic choroidal neovascularization (CNV) in a pediatric patient successfully treated with intravitreal bevacizumab injections.  Methods: case report of a 10 year-old patient, who presented with reduced unilateral visual acuity during a visual screening. Complete ophthalmological examination was performed, along with fluorescein angiography, spectral domain optic coherence tomography (SD-OCT), fundus autofluorescence, ocular ultrasound, magnetic resonance imaging (MRI) of the brain and orbits and infectious serologies. Results: visual acuity was 20/400 in the left eye (OS) and 20/20 in the right eye (OD). No significant refractive error was detected. Fundoscopy in OS revealed a subretinal macular lesion associated with subretinal hemorrhage and fluid. Fluorescein angiography and SD-OCT confirmed the presence of NVC. Retinal hereditary dystrophies, along with infectious and neoplastic causes were excluded. The patient underwent two intravitreal bevacizumab injections in OS with a 3 months interval. Treatment resulted in progressive fibrosis of NVC, resolution of subretinal fluid and improvement of visual acuity in OS to 20/125, which remained stable 4 years after treatment. Conclusions: In the case of pediatric NVC, retinal hereditary dystrophies along with infectious and neoplastic causes should be excluded after a thorough investigation. No standard treatment for CNV in children has yet been validated. In our patient anti-vascular endothelial growth factor (VEGF) treatment induced regression of the CNV and resolution of subretinal fluid with a modest recovery in visual acuity and no reported ocular or systemic side effects. Ajnet2018-12-11T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/reporthttps://doi.org/10.48560/rspo.13416eng1646-69501646-6950Couceiro, RitaAmaro, MiguelFerreira, AnaCavalheiro, Diogoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-22T17:06:04Zoai:ojs.revistas.rcaap.pt:article/13416Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:01:41.056280Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
title Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
spellingShingle Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
Couceiro, Rita
Comunicações Curtas e Imagens em Oftalmologia
title_short Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
title_full Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
title_fullStr Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
title_full_unstemmed Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
title_sort Idiopathic choroidal neovascularization in a 10 year-old child treated with intravitreal bevacizumab injections
author Couceiro, Rita
author_facet Couceiro, Rita
Amaro, Miguel
Ferreira, Ana
Cavalheiro, Diogo
author_role author
author2 Amaro, Miguel
Ferreira, Ana
Cavalheiro, Diogo
author2_role author
author
author
dc.contributor.author.fl_str_mv Couceiro, Rita
Amaro, Miguel
Ferreira, Ana
Cavalheiro, Diogo
dc.subject.por.fl_str_mv Comunicações Curtas e Imagens em Oftalmologia
topic Comunicações Curtas e Imagens em Oftalmologia
description Purpose: to report a case of idiopathic choroidal neovascularization (CNV) in a pediatric patient successfully treated with intravitreal bevacizumab injections.  Methods: case report of a 10 year-old patient, who presented with reduced unilateral visual acuity during a visual screening. Complete ophthalmological examination was performed, along with fluorescein angiography, spectral domain optic coherence tomography (SD-OCT), fundus autofluorescence, ocular ultrasound, magnetic resonance imaging (MRI) of the brain and orbits and infectious serologies. Results: visual acuity was 20/400 in the left eye (OS) and 20/20 in the right eye (OD). No significant refractive error was detected. Fundoscopy in OS revealed a subretinal macular lesion associated with subretinal hemorrhage and fluid. Fluorescein angiography and SD-OCT confirmed the presence of NVC. Retinal hereditary dystrophies, along with infectious and neoplastic causes were excluded. The patient underwent two intravitreal bevacizumab injections in OS with a 3 months interval. Treatment resulted in progressive fibrosis of NVC, resolution of subretinal fluid and improvement of visual acuity in OS to 20/125, which remained stable 4 years after treatment. Conclusions: In the case of pediatric NVC, retinal hereditary dystrophies along with infectious and neoplastic causes should be excluded after a thorough investigation. No standard treatment for CNV in children has yet been validated. In our patient anti-vascular endothelial growth factor (VEGF) treatment induced regression of the CNV and resolution of subretinal fluid with a modest recovery in visual acuity and no reported ocular or systemic side effects. 
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T00:00:00Z
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