Literature DB >> 19683192

Ocular findings in childhood-onset Behçet disease.

Mehmet Citirik1, Nilufer Berker, Murat Serkan Songur, Emel Soykan, Orhan Zilelioglu.   

Abstract

PURPOSE: To investigate the demographic characteristics and ocular features of patients with childhood-onset Behçet disease. PATIENTS AND METHODS: Patients for this retrospective study were selected using the data obtained from medical records of 34 patients with childhood-onset Behçet disease being followed up in the Uveitis Department of Ankara Ulucanlar Eye Education and Research Hospital between January 2003 and May 2008.
RESULTS: Of 34 patients, 24 were boys (70.5%) and 10 were girls (29.4%). The average age of patients was 14.5 +/- 1.9 years (range, 10-16 years). Mean follow-up period was 4.5 +/- 2 years (range, 2-10 years). During the follow-up, panuveitis, posterior uveitis, and anterior uveitis were diagnosed in 18 (52.9%), 11 (32.3%), and 5 (14.7%) patients, respectively. Ocular findings included cataract in 20 patients (58.8%), posterior synechiae in 8 (23.5%), posterior capsular opacification secondary to cataract surgery in 8 (23.5%), vitreous condensation due to previous episodes of vitritis in 17 (50%), optic atrophy in 10 (29.4%), cystoid macular edema in 5 patients (14.7%), narrowed and occluded retinal vessels due to retinal periphlebitis and branched retinal vein occlusion in 2 (5.8%), neovascularization of the disk in 1 (2.9%), and phthisis bulbi in 1 patient (2.9%).
CONCLUSIONS: Based on the results that were obtained in this series, panuveitis was the most common type of uveitis in cases with childhood-onset Behçet disease. Cataract was the most common anterior segment complication. Optic atrophy was the most common posterior segment complication. Male predominance was determined in this study.

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Year:  2009        PMID: 19683192     DOI: 10.1016/j.jaapos.2009.04.016

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  8 in total

1.  Platelet Activation in Ocular Behçet's Patients with Posterior Segment Involvement.

Authors:  Mehmet Citirik; Pinar C Ozdal; Ali Keles; Ibrahim C Haznedaroglu
Journal:  Middle East Afr J Ophthalmol       Date:  2022-04-30

Review 2.  Current perspectives on ophthalmic manifestations of childhood rheumatic diseases.

Authors:  Neal V Palejwala; Steven Yeh; Sheila T Angeles-Han
Journal:  Curr Rheumatol Rep       Date:  2013-07       Impact factor: 4.592

3.  Pediatric uveitis.

Authors:  Ilknur Tugal-Tutkun
Journal:  J Ophthalmic Vis Res       Date:  2011-10

4.  Paediatric Behçet's disease presenting with recurrent papillitis and episcleritis: a case report.

Authors:  Fulvio Parentin; Loredana Lepore; Ingrid Rabach; Stefano Pensiero
Journal:  J Med Case Rep       Date:  2011-02-25

Review 5.  Behçet's Disease in Children: Diagnostic and Management Challenges.

Authors:  Giorgio Costagliola; Susanna Cappelli; Rita Consolini
Journal:  Ther Clin Risk Manag       Date:  2020-06-11       Impact factor: 2.423

6.  Behcet's Disease Presenting With Bilateral Hypopyon Masquerading Post Cataract Surgery Endophthalmitis.

Authors:  Mehrdad Mohammadpour; Meysam Kosari; Masoud Khorrami-Nejad
Journal:  Int Med Case Rep J       Date:  2019-11-28

Review 7.  Behçet uveitis: Current practice and future perspectives.

Authors:  Shereen H Aboul Naga; Lameece Moustafa Hassan; Radwa T El Zanaty; Mohammad Refaat; Rana H Amin; Gaafar Ragab; Mahmoud M Soliman
Journal:  Front Med (Lausanne)       Date:  2022-09-07

Review 8.  Neuro-Behçet's disease in childhood: a focus on the neuro-ophthalmological features.

Authors:  Paolo Mora; Chiara Menozzi; Jelka G Orsoni; Pierangela Rubino; Livia Ruffini; Arturo Carta
Journal:  Orphanet J Rare Dis       Date:  2013-01-29       Impact factor: 4.123

  8 in total

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