Literature DB >> 24661864

Stellate nonhereditary idiopathic foveomacular retinoschisis.

Michael D Ober1, K Bailey Freund2, Manthan Shah3, Shareef Ahmed3, Tamer H Mahmoud4, Thomas M Aaberg5, David N Zacks6, Hua Gao3, Krishna Mukkamala2, Uday Desai3, Kirk H Packo7, Lawrence A Yannuzzi2.   

Abstract

PURPOSE: To describe a new classification of stellate nonhereditary idiopathic foveomacular retinoschisis (SNIFR).
DESIGN: Retrospective case series and literature review. PARTICIPANTS: A total of 17 patients from 5 institutions.
METHODS: Detailed case history, multimodal imaging, and genetic testing were reviewed for patients with macular schisis without a known predisposing condition. Patients with a stellate appearance centered on the fovea with correlating confirmed expansion of the outer plexiform layer (OPL) by optical coherence tomography (OCT) were included. Exclusion criteria included a family history of macular retinoschisis, a known genetic abnormality associated with retinoschisis, myopic traction maculopathy, epiretinal membrane, vitreoretinal traction, optic or scleral pit, or advanced glaucomatous optic nerve changes. MAIN OUTCOME MEASURES: Clinical features, anatomic characteristics, and visual acuity.
RESULTS: A total of 22 eyes from 16 female patients and 1 male patient with foveomacular schisis were reviewed from 5 institutions. Initial visual acuity was ≥ 20/50 in all eyes (mean, 20/27), but visual acuity in a single eye decreased from 20/20 to 20/200 after the development of subfoveal fluid. The refractive status was myopic in 16 eyes, plano in 3 eyes, and hyperopic in 2 eyes. Three eyes had a preexisting vitreous separation, and 19 eyes had an attached posterior hyaloid. Follow-up ranged from 6 months to >5 years.
CONCLUSIONS: In this largest known series of patients with SNIFR, all patients demonstrated splitting of the OPL in the macula with relatively preserved visual acuity (≥ 20/40) except in a single patient in whom subretinal fluid developed under the fovea.
Copyright © 2014. Published by Elsevier Inc.

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Year:  2014        PMID: 24661864     DOI: 10.1016/j.ophtha.2014.02.002

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  6 in total

1.  Stellate nonhereditary idiopathic foveomacular retinoschisis concomitant to exudative maculopathies.

Authors:  G Casalino; M Upendran; F Bandello; U Chakravarthy
Journal:  Eye (Lond)       Date:  2016-02-26       Impact factor: 3.775

2.  AN ASSOCIATION BETWEEN STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS, PERIPHERAL RETINOSCHISIS, AND POSTERIOR HYALOID ATTACHMENT.

Authors:  Edward Bloch; Blanca Flores-Sánchez; Odysseas Georgiadis; Venki Sundaram; Zubin Saihan; Omar A Mahroo; Andrew R Webster; Lyndon da Cruz
Journal:  Retina       Date:  2021-11-01       Impact factor: 4.256

3.  Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis: Cataract Surgery.

Authors:  Sofie Van der Auwera; Oscar Kallay
Journal:  Case Rep Ophthalmol Med       Date:  2022-09-09

4.  Multimodal imaging in a case of stellate nonhereditary idiopathic foveomacular retinoschisis.

Authors:  Divya Yadav; Pankaja Dhoble; Nikita Sonawane; Santosh Ramesh
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

5.  Stellate nonhereditary idiopathic foveomacular retinoschisis resolution after vitreomacular adhesion release.

Authors:  Thiago Machado Nogueira; Daniel de Souza Costa; Jordan Isenberg; Flavio A Rezende
Journal:  Am J Ophthalmol Case Rep       Date:  2021-06-19

6.  Retinoschisis associated with Kearns-Sayre syndrome.

Authors:  Julia Chertkof; Robert B Hufnagel; Delphine Blain; Andrea L Gropman; Brian P Brooks
Journal:  Ophthalmic Genet       Date:  2020-08-13       Impact factor: 1.803

  6 in total

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