Blepharokeratoconjunctivitis in children: diagnosis and treatment

Aim: Blepharokeratoconjunctivitis (BKC) is a poorly described entity in children. This study characterises this syndrome in childhood and evaluates epidemiology, clinical grading, and treatment strategies. Methods: 44 children (20 white, 22 Asian, 2 Middle Eastern, median age 5.4 (range 1–14) years)...

Full description

Saved in:
Bibliographic Details
Published inBritish journal of ophthalmology Vol. 89; no. 4; pp. 400 - 403
Main Authors Viswalingam, M, Rauz, S, Morlet, N, Dart, J K G
Format Journal Article
LanguageEnglish
Published BMA House, Tavistock Square, London, WC1H 9JR BMJ Publishing Group Ltd 01.04.2005
BMJ
BMJ Publishing Group LTD
Copyright 2005 British Journal of Ophthalmology
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Aim: Blepharokeratoconjunctivitis (BKC) is a poorly described entity in children. This study characterises this syndrome in childhood and evaluates epidemiology, clinical grading, and treatment strategies. Methods: 44 children (20 white, 22 Asian, 2 Middle Eastern, median age 5.4 (range 1–14) years) with a diagnosis of BKC were followed for a median of 7 years. Diagnostic criteria included recurrent episodes of chronic red eye, watering, photophobia, blepharitis including recurrent styes or meibomian cysts, and a keratitis. Clinical features were graded as mild, moderate, or severe. The lids and conjunctiva were cultured. The treatment regimen incorporated lid hygiene, topical and/or systemic antibiotics, and topical corticosteroids. Results: The disease was most severe in the Asian and Middle Eastern children (p <0.001), who had a statistically higher risk of subepithelial punctate keratitis (p = 0.008), corneal vascularisation (p <0.001), and marginal corneal ulcerations (p = 0.003), than the white group. 15 children had culture positive lid swabs. Most children had a reduction in symptoms and signs with treatment, and progression of disease after the age of 8 was rare. Conclusions: BKC in children can be defined as “a syndrome usually associated with anterior or posterior lid margin blepharitis, accompanied by episodes of conjunctivitis, and a keratopathy including punctate erosions, punctate keratitis, phlyctenules, marginal keratitis, and ulceration.” BKC is common in children in a tertiary referral corneal and external diseases clinic, with the more severe manifestations in the Asian and Middle Eastern populations. Therapy is effective and loss of sight can be prevented in most cases.
Bibliography:istex:4271D94E173AF029FDCFF8A79D5E7651E7367019
ark:/67375/NVC-8STR0WNX-1
href:bjophthalmol-89-400.pdf
PMID:15774912
Correspondence to: John K G Dart Corneal and External Diseases Service, Moorfields Eye Hospital NHS Trust, 162 City Road, London EC1V 2PD, UK; j.dart@ucl.ac.uk
local:0890400
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
The authors have no proprietary interest in the products described in this article.
Correspondence to: …John K G Dart …Corneal and External Diseases Service, Moorfields Eye Hospital NHS Trust, 162 City Road, London EC1V 2PD, UK; j.dart@ucl.ac.uk
ISSN:0007-1161
1468-2079
DOI:10.1136/bjo.2004.052134