Literature DB >> 20419849

Macular fibrosis in Coats disease.

J Michael Jumper1, Dustin Pomerleau, H Richard McDonald, Robert N Johnson, Arthur D Fu, Emmett T Cunningham.   

Abstract

PURPOSE: The purpose of this study was to describe the angiographic features and visual impact of macular fibrosis in patients with Coats disease.
METHODS: This is a single institution retrospective case series. Charts of patients diagnosed with Coats disease between 1973 and 2007 were reviewed. Data collected included patient demographics, treatment method, initial and final logarithm of the minimum angle of resolution visual acuity, photographic findings, angiographic characteristics, and anatomical outcome.
RESULTS: Forty-seven patients were identified with adequate imaging and posttreatment follow-up. Average age at presentation was 38 years (4-82 years). Average follow-up was 4.9 years (0-17 years). Macular fibrosis was identified in 11 patients (23%). At presentation, the average logarithm of the minimum angle of resolution visual acuity was as follows: all patients, 0.67; patients with macular fibrosis, 1.14; and patients without macular fibrosis, 0.50 (P = 0.01, 2-tailed Student's t-test). The average posttreatment logarithm of the minimum angle of resolution visual acuity was as follows: all patients, 0.78; patients with macular fibrosis, 0.97; and patients without macular fibrosis, 0.70 (P = 0.26). Macular fibrosis was associated with a pigmented spot at the point of apparent intraretinal vascular anastamosis. Fluorescein angiography showed leakage consistent with neovascularization that appeared to be intraretinal.
CONCLUSION: Macular fibrosis is a common finding in Coats disease, occurring in 23% of our patients. It may be a result of intraretinal neovascularization and is associated with a worse vision outcome.

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Year:  2010        PMID: 20419849     DOI: 10.1097/iae.0b013e3181cfd3e7

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  7 in total

1.  Comparison of Optical Coherence Tomography With Fundus Photographs, Fluorescein Angiography, and Histopathologic Analysis in Assessing Coats Disease.

Authors:  Sally S Ong; Thomas J Cummings; Lejla Vajzovic; Prithvi Mruthyunjaya; Cynthia A Toth
Journal:  JAMA Ophthalmol       Date:  2019-02-01       Impact factor: 7.389

Review 2.  Paediatric retinal detachment: a review.

Authors:  Raffaele Nuzzi; Carlo Lavia; Roberta Spinetta
Journal:  Int J Ophthalmol       Date:  2017-10-18       Impact factor: 1.779

3.  Long-term follow-up of a case of Coats disease in a 10-year-old boy with spontaneous peeling of preretinal macular fibrosis: a case report.

Authors:  Tomoka Mizobuchi; Takashi Nishiuchi; Yusaku Miura; Ken Fukuda
Journal:  BMC Ophthalmol       Date:  2022-04-27       Impact factor: 2.086

4.  SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis.

Authors:  Alejandra L Daruich; Alexandre P Moulin; Hoai V Tran; Alexandre Matet; Francis L Munier
Journal:  Retina       Date:  2017-08       Impact factor: 4.256

5.  Adult Coats Disease Presenting as Subfoveal Nodule.

Authors:  Salim Z Asaad; Nazimul Hussain
Journal:  Case Rep Ophthalmol       Date:  2018-03-22

6.  Macular Features on Spectral-Domain Optical Coherence Tomography Imaging Associated With Visual Acuity in Coats' Disease.

Authors:  Sally S Ong; Prithvi Mruthyunjaya; Sandra Stinnett; Lejla Vajzovic; Cynthia A Toth
Journal:  Invest Ophthalmol Vis Sci       Date:  2018-06-01       Impact factor: 4.799

7.  A Case of Congenital Simple Hamartoma of the Retinal Pigment Epithelium and Coats' Disease in the Same Eye.

Authors:  Won Jae Heo; Dong Ho Park; Jae Pil Shin
Journal:  Korean J Ophthalmol       Date:  2015-08
  7 in total

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