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Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia

OBJECTIVES: To evaluate the vascular changes of idiopathic macular telangiectasia type 2 (MacTel 2) patients with optical coherence tomography angiography (OCTA) and correlate these changes with the findings of spectral domain optical coherence tomography (SD-OCT). MATERIALS AND METHODS: Simultaneou...

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Autores principales: Nalcı, Hilal, Şermet, Figen, Demirel, Sibel, Özmert, Emin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661178/
https://www.ncbi.nlm.nih.gov/pubmed/29109897
http://dx.doi.org/10.4274/tjo.68335
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author Nalcı, Hilal
Şermet, Figen
Demirel, Sibel
Özmert, Emin
author_facet Nalcı, Hilal
Şermet, Figen
Demirel, Sibel
Özmert, Emin
author_sort Nalcı, Hilal
collection PubMed
description OBJECTIVES: To evaluate the vascular changes of idiopathic macular telangiectasia type 2 (MacTel 2) patients with optical coherence tomography angiography (OCTA) and correlate these changes with the findings of spectral domain optical coherence tomography (SD-OCT). MATERIALS AND METHODS: Simultaneous SD-OCT and OCTA images of 10 eyes of 6 patients who were diagnosed as MacTel 2 in Ankara University Faculty of Medicine, Department of Ophthalmology were obtained and graded according to the OCTA grading system for MacTel 2. RESULTS: Ten eyes of 6 patients were included. Four (66%) patients were female and 2 (34%) were male. The disease was grade 0 in 2 eyes, grade 1 in 2 eyes, grade 2 in 3 eyes, grade 3 in 1 eye, grade 4 in 1 eye, and grade 5 in 1 eye. The most common findings in grade 1, 2, and 3 non-proliferative disease were thinning of the outer retinal layers, presence of intraretinal hyporeflective layers and inner limiting membrane draping. In cases with subretinal choroidal neovascularisation (CNV) in OCTA, CNV or CNV scar was present in the B-scan SD-OCT images. In a case in which OCT was within normal limits, vascular changes consistent with grade 1 disease were observed in OCTA. On the contrary, 2 patients with significant foveal atrophy and macular hole in B-scan showed changes of early disease in OCTA. In some of the eyes, OCTA revealed an intact superficial vascular layer despite visible changes in the deep layer and the presence of neovascularisation. CONCLUSION: OCTA yields findings which are important for understanding the pathogenesis of the disease and providing better follow-up. Contrary to fundus fluorescein angiography, changes in the deep arterial plexus in the early disease and CNV can be clearly observed with OCTA. To achieve the best results in clinical practice, en face flow maps should be evaluated together with B-scan SD-OCT images.
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spelling pubmed-56611782017-11-06 Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia Nalcı, Hilal Şermet, Figen Demirel, Sibel Özmert, Emin Turk J Ophthalmol Original Article OBJECTIVES: To evaluate the vascular changes of idiopathic macular telangiectasia type 2 (MacTel 2) patients with optical coherence tomography angiography (OCTA) and correlate these changes with the findings of spectral domain optical coherence tomography (SD-OCT). MATERIALS AND METHODS: Simultaneous SD-OCT and OCTA images of 10 eyes of 6 patients who were diagnosed as MacTel 2 in Ankara University Faculty of Medicine, Department of Ophthalmology were obtained and graded according to the OCTA grading system for MacTel 2. RESULTS: Ten eyes of 6 patients were included. Four (66%) patients were female and 2 (34%) were male. The disease was grade 0 in 2 eyes, grade 1 in 2 eyes, grade 2 in 3 eyes, grade 3 in 1 eye, grade 4 in 1 eye, and grade 5 in 1 eye. The most common findings in grade 1, 2, and 3 non-proliferative disease were thinning of the outer retinal layers, presence of intraretinal hyporeflective layers and inner limiting membrane draping. In cases with subretinal choroidal neovascularisation (CNV) in OCTA, CNV or CNV scar was present in the B-scan SD-OCT images. In a case in which OCT was within normal limits, vascular changes consistent with grade 1 disease were observed in OCTA. On the contrary, 2 patients with significant foveal atrophy and macular hole in B-scan showed changes of early disease in OCTA. In some of the eyes, OCTA revealed an intact superficial vascular layer despite visible changes in the deep layer and the presence of neovascularisation. CONCLUSION: OCTA yields findings which are important for understanding the pathogenesis of the disease and providing better follow-up. Contrary to fundus fluorescein angiography, changes in the deep arterial plexus in the early disease and CNV can be clearly observed with OCTA. To achieve the best results in clinical practice, en face flow maps should be evaluated together with B-scan SD-OCT images. Galenos Publishing 2017-10 2017-10-27 /pmc/articles/PMC5661178/ /pubmed/29109897 http://dx.doi.org/10.4274/tjo.68335 Text en © Copyright 2017 by Turkish Ophthalmological Association Turkish Journal of Ophthalmology, published by Galenos Publishing House. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Nalcı, Hilal
Şermet, Figen
Demirel, Sibel
Özmert, Emin
Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia
title Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia
title_full Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia
title_fullStr Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia
title_full_unstemmed Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia
title_short Optic Coherence Angiography Findings in Type-2 Macular Telangiectasia
title_sort optic coherence angiography findings in type-2 macular telangiectasia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661178/
https://www.ncbi.nlm.nih.gov/pubmed/29109897
http://dx.doi.org/10.4274/tjo.68335
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