Literature DB >> 30563364

Glaucoma in children with facial port wine stain.

Nader Hussein Lotfy Bayoumi1, Eman Nabil Elsayed1.   

Abstract

PURPOSE: To report on the clinical presentation and surgical treatment (procedure and outcome(s)) of glaucoma in children with facial port wine stain.
MATERIALS AND METHODS: This is a retrospective chart review of children with facial port wine stain referred to Alexandria University paediatric ophthalmology practice from 2005 to 2016. The charts of 22 children (44 eyes) with facial port wine stain were reviewed. The data extracted included demographics, results of ophthalmic examination findings and treatment(s). The main outcome measures were the number of eyes stratified as glaucoma, glaucoma suspects and no glaucoma at the initial and final presentations.
RESULTS: The average age of presentation was 18.2 (±33.9) months. After a follow-up of over 16.1 (±24.8) months, there were 34%, 30% and 36% of the study eyes diagnosed as glaucoma, glaucoma suspects and no glaucoma, respectively with mean ± standard deviation of intraocular pressure of 20.6 ± 5.1, 13.6 ± 5.4 and 7.5 ± 1.7 mmHg. The majority (91%) of eyes presenting with glaucoma had clear corneas. In total, 11 eyes were operated upon for glaucoma. The recorded success rate was 91%. Two eyes developed a postoperative exudative choroidal detachment, of which one resolved spontaneously and the other was successfully managed by intravitreal gas injection.
CONCLUSION: Glaucoma is a significant ocular hazard in children with facial port wine stain that may not be evident on the initial presentation. The presentation is usually with a clear cornea and surgical intervention is associated with a high success rate and a low rate of complications.

Entities:  

Keywords:  Glaucoma; Sturge–Weber syndrome; children; trabeculectomy; trabeculotomy

Mesh:

Year:  2018        PMID: 30563364     DOI: 10.1177/1120672118819668

Source DB:  PubMed          Journal:  Eur J Ophthalmol        ISSN: 1120-6721            Impact factor:   2.597


  4 in total

1.  Asymmetric cavernous sinus enlargement: a novel finding in Sturge-Weber syndrome.

Authors:  Luca Pasquini; Domenico Tortora; Francesca Manunza; Maria Camilla Rossi Espagnet; Lorenzo Figà-Talamanca; Giovanni Morana; Corrado Occella; Andrea Rossi; Mariasavina Severino
Journal:  Neuroradiology       Date:  2019-02-12       Impact factor: 2.804

2.  Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge-Weber Syndrome.

Authors:  Li Li; Tianwei Liang; Honggai Yan; Man Hu; Yanhui Cui
Journal:  BMC Ophthalmol       Date:  2022-06-09       Impact factor: 2.086

3.  Clinical outcome measures and scoring systems used in prospective studies of port wine stains: A systematic review.

Authors:  M Ingmar van Raath; Sandeep Chohan; Albert Wolkerstorfer; Chantal M A M van der Horst; Jacqueline Limpens; Xuan Huang; Baoyue Ding; Gert Storm; René R W J van der Hulst; Michal Heger
Journal:  PLoS One       Date:  2020-07-02       Impact factor: 3.240

4.  Progressive retinal vessel malformation in a premature infant with Sturge-Weber syndrome: a case report and a literature review of ocular manifestations in Sturge-Weber syndrome.

Authors:  Zhengping Hu; Jian Cao; Eun Young Choi; Yun Li
Journal:  BMC Ophthalmol       Date:  2021-01-22       Impact factor: 2.209

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.