CONCURRENT IDIOPATHIC MACULAR TELANGIECTASIA TYPE 2 AND CENTRAL SEROUS CHORIORETINOPATHY.

Détails

ID Serval
serval:BIB_62FBFB0A1B0C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
CONCURRENT IDIOPATHIC MACULAR TELANGIECTASIA TYPE 2 AND CENTRAL SEROUS CHORIORETINOPATHY.
Périodique
Retina
Auteur⸱e⸱s
Matet A., Yzer S., Chew E.Y., Daruich A., Behar-Cohen F., Spaide R.F.
ISSN
1539-2864 (Electronic)
ISSN-L
0275-004X
Statut éditorial
Publié
Date de publication
01/2018
Peer-reviewed
Oui
Volume
38 Suppl 1
Pages
S67-S78
Langue
anglais
Notes
Publication types: Journal Article ; Multicenter Study ; Observational Study
Publication Status: ppublish
Résumé
To describe cases presenting with features of idiopathic macular telangiectasia (MacTel) Type 2 and central serous chorioretinopathy (CSC).
Databases from four tertiary retina centers were searched for cases copresenting CSC and MacTel Type 2.
Five cases were identified (4 men, 1 woman; mean age: 67.2 years). Four patients were referred for chronic or nonresolving CSC, and the diagnosis of MacTel Type 2 was made based on multimodal imaging findings. One patient had advanced MacTel Type 2, and developed acute CSC. Regarding the MacTel Type 2 findings, all subjects presented perifoveal telangiectasia on fluorescein angiography, and four subjects showed intraretinal cavitations typical of MacTel Type 2 on optical coherence tomography, in one or both eyes. Regarding the CSC findings, fluorescein angiography identified focal or extended retinal pigment epithelium alteration in all eyes, and an active leakage in two eyes. Indocyanine green angiography showed choroidal vascular hyperpermeability in four subjects. On optical coherence tomography, pigment epithelial detachments were detected in five eyes (four subjects), and foveal detachments were present in five eyes (three subjects), which spontaneously resolved (two eyes), responded to photodynamic therapy (two eyes), or persisted (one eye). Mean choroidal thickness was 402 ± 99 μm.
The codiagnosis of CSC and MacTel Type 2 should be considered in atypical presentations associating features from both disorders.
Mots-clé
Aged, Central Serous Chorioretinopathy/complications, Central Serous Chorioretinopathy/diagnosis, Central Serous Chorioretinopathy/physiopathology, Choroid/pathology, Female, Fluorescein Angiography/methods, Follow-Up Studies, Fundus Oculi, Humans, Macula Lutea/pathology, Male, Middle Aged, Retina, Retrospective Studies, Telangiectasia, Hereditary Hemorrhagic/complications, Telangiectasia, Hereditary Hemorrhagic/diagnosis, Telangiectasia, Hereditary Hemorrhagic/physiopathology, Tomography, Optical Coherence/methods, Visual Acuity
Pubmed
Web of science
Création de la notice
10/03/2018 12:09
Dernière modification de la notice
20/08/2019 15:19
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