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Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia

Purpose. To report unusual presentation of type 1A idiopathic macular telangiectasia (IMT). Methods. Two middle-aged women with bilateral IMT were examined. Results. Both patients presented with a gradual vision loss in both eyes. Fundus examination was unremarkable in one case and showed small macu...

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Autores principales: Bentaleb Machkour, Zaïnab, Denis, Philippe, Kodjikian, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288508/
https://www.ncbi.nlm.nih.gov/pubmed/28203470
http://dx.doi.org/10.1155/2017/5395069
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author Bentaleb Machkour, Zaïnab
Denis, Philippe
Kodjikian, Laurent
author_facet Bentaleb Machkour, Zaïnab
Denis, Philippe
Kodjikian, Laurent
author_sort Bentaleb Machkour, Zaïnab
collection PubMed
description Purpose. To report unusual presentation of type 1A idiopathic macular telangiectasia (IMT). Methods. Two middle-aged women with bilateral IMT were examined. Results. Both patients presented with a gradual vision loss in both eyes. Fundus examination was unremarkable in one case and showed small macular telangiectasia in both eyes in the other case. Fluorescein angiography (FA) revealed early bilateral macular punctuated hyperfluorescence corresponding to the dilated capillaries in both cases. FA and fundus examination confirmed also the absence of vascular abnormalities in the middle or anterior fundus periphery in one case. Spectral-domain optical coherence tomography (SD-OCT) showed cystoid macular edema in both cases. No signs of retinal vein occlusions were detected in both cases and other differential diagnoses were excluded. Based on these findings, the patients were diagnosed with bilateral type 1A IMT according to Gass and Blodi classification and were treated with intravitreal antivascular endothelial growth factor (anti-VEGF) injections and focal laser photocoagulation. Twelve months later, SD-OCT revealed partial regression of the exudative signs and significant VA improvement. Conclusion. We described two patients with an unusual presentation of type 1A IMT with bilateral presentation, affecting two middle-aged women, with occult and without peripheral involvement in one case. The description of more cases of bilateral type 1 IMT should be helpful to more precisely define the pathophysiologic mechanism that could be different from a localized Coats' disease of the macula area.
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spelling pubmed-52885082017-02-15 Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia Bentaleb Machkour, Zaïnab Denis, Philippe Kodjikian, Laurent Case Rep Ophthalmol Med Case Report Purpose. To report unusual presentation of type 1A idiopathic macular telangiectasia (IMT). Methods. Two middle-aged women with bilateral IMT were examined. Results. Both patients presented with a gradual vision loss in both eyes. Fundus examination was unremarkable in one case and showed small macular telangiectasia in both eyes in the other case. Fluorescein angiography (FA) revealed early bilateral macular punctuated hyperfluorescence corresponding to the dilated capillaries in both cases. FA and fundus examination confirmed also the absence of vascular abnormalities in the middle or anterior fundus periphery in one case. Spectral-domain optical coherence tomography (SD-OCT) showed cystoid macular edema in both cases. No signs of retinal vein occlusions were detected in both cases and other differential diagnoses were excluded. Based on these findings, the patients were diagnosed with bilateral type 1A IMT according to Gass and Blodi classification and were treated with intravitreal antivascular endothelial growth factor (anti-VEGF) injections and focal laser photocoagulation. Twelve months later, SD-OCT revealed partial regression of the exudative signs and significant VA improvement. Conclusion. We described two patients with an unusual presentation of type 1A IMT with bilateral presentation, affecting two middle-aged women, with occult and without peripheral involvement in one case. The description of more cases of bilateral type 1 IMT should be helpful to more precisely define the pathophysiologic mechanism that could be different from a localized Coats' disease of the macula area. Hindawi Publishing Corporation 2017 2017-01-19 /pmc/articles/PMC5288508/ /pubmed/28203470 http://dx.doi.org/10.1155/2017/5395069 Text en Copyright © 2017 Zaïnab Bentaleb Machkour 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
Bentaleb Machkour, Zaïnab
Denis, Philippe
Kodjikian, Laurent
Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia
title Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia
title_full Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia
title_fullStr Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia
title_full_unstemmed Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia
title_short Unusual Presentation of Type 1 Idiopathic Macular Telangiectasia
title_sort unusual presentation of type 1 idiopathic macular telangiectasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288508/
https://www.ncbi.nlm.nih.gov/pubmed/28203470
http://dx.doi.org/10.1155/2017/5395069
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