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Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane

Purpose. To describe the case of spontaneous resolution of epiretinal membrane in a patient with Combined Hamartoma of the Retina and Retinal Pigment Epithelium (CHR-RPE), in the clinical context of Gorlin Syndrome (GS). Methods. Observational case report of a 12-year-old female patient is presented...

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Autores principales: Sánchez-Vicente, José L., Contreras-Díaz, Miguel, Rueda, Trinidad, Rodríguez de la Rúa-Franch, Enrique, Molina-Socola, Fredy E., Vital-Berral, Cristina, Alfaro-Juárez, Asunción, López-Herrero, Fernando, Muñoz-Morales, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993932/
https://www.ncbi.nlm.nih.gov/pubmed/27595027
http://dx.doi.org/10.1155/2016/2312196
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author Sánchez-Vicente, José L.
Contreras-Díaz, Miguel
Rueda, Trinidad
Rodríguez de la Rúa-Franch, Enrique
Molina-Socola, Fredy E.
Vital-Berral, Cristina
Alfaro-Juárez, Asunción
López-Herrero, Fernando
Muñoz-Morales, Ana
author_facet Sánchez-Vicente, José L.
Contreras-Díaz, Miguel
Rueda, Trinidad
Rodríguez de la Rúa-Franch, Enrique
Molina-Socola, Fredy E.
Vital-Berral, Cristina
Alfaro-Juárez, Asunción
López-Herrero, Fernando
Muñoz-Morales, Ana
author_sort Sánchez-Vicente, José L.
collection PubMed
description Purpose. To describe the case of spontaneous resolution of epiretinal membrane in a patient with Combined Hamartoma of the Retina and Retinal Pigment Epithelium (CHR-RPE), in the clinical context of Gorlin Syndrome (GS). Methods. Observational case report of a 12-year-old female patient is presented. The diagnosis of CHRRPE was made by OCT and fundus examination, which showed a mound of disorganized tissue originating from retina and retinal pigment epithelium. Epiretinal membrane (EM) was also detected. Genetic study was performed to confirm the diagnosis of GS. Results. The patient was observed for 39 months, showing spontaneous resolution of the traction caused by the EM and improvement in visual acuity (VA), which was 20/80 at initial presentation, rising to 20/40 after follow-up period. Conclusions. The presence of EM in CHR-REP is a cause of reduction of visual acuity. Management of this condition is controversial; however, we would like to highlight that spontaneous resolution of the traction caused by EM is possible, resulting in recovery of VA.
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spelling pubmed-49939322016-09-04 Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane Sánchez-Vicente, José L. Contreras-Díaz, Miguel Rueda, Trinidad Rodríguez de la Rúa-Franch, Enrique Molina-Socola, Fredy E. Vital-Berral, Cristina Alfaro-Juárez, Asunción López-Herrero, Fernando Muñoz-Morales, Ana Case Rep Ophthalmol Med Case Report Purpose. To describe the case of spontaneous resolution of epiretinal membrane in a patient with Combined Hamartoma of the Retina and Retinal Pigment Epithelium (CHR-RPE), in the clinical context of Gorlin Syndrome (GS). Methods. Observational case report of a 12-year-old female patient is presented. The diagnosis of CHRRPE was made by OCT and fundus examination, which showed a mound of disorganized tissue originating from retina and retinal pigment epithelium. Epiretinal membrane (EM) was also detected. Genetic study was performed to confirm the diagnosis of GS. Results. The patient was observed for 39 months, showing spontaneous resolution of the traction caused by the EM and improvement in visual acuity (VA), which was 20/80 at initial presentation, rising to 20/40 after follow-up period. Conclusions. The presence of EM in CHR-REP is a cause of reduction of visual acuity. Management of this condition is controversial; however, we would like to highlight that spontaneous resolution of the traction caused by EM is possible, resulting in recovery of VA. Hindawi Publishing Corporation 2016 2016-08-09 /pmc/articles/PMC4993932/ /pubmed/27595027 http://dx.doi.org/10.1155/2016/2312196 Text en Copyright © 2016 José L. Sánchez-Vicente et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sánchez-Vicente, José L.
Contreras-Díaz, Miguel
Rueda, Trinidad
Rodríguez de la Rúa-Franch, Enrique
Molina-Socola, Fredy E.
Vital-Berral, Cristina
Alfaro-Juárez, Asunción
López-Herrero, Fernando
Muñoz-Morales, Ana
Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane
title Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane
title_full Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane
title_fullStr Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane
title_full_unstemmed Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane
title_short Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane
title_sort combined hamartoma of the retina and retinal pigment epithelium in a patient with gorlin syndrome: spontaneous partial resolution of traction caused by epiretinal membrane
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993932/
https://www.ncbi.nlm.nih.gov/pubmed/27595027
http://dx.doi.org/10.1155/2016/2312196
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