Literature DB >> 29998839

Paediatric Behçet's disease in Iran: report of 204 cases.

Farhad Shahram1, Abdolhadi Nadji2, Massoomeh Akhlaghi3, Seyyedeh Tahereh Faezi3, Cheyda Chams-Davatchi4, Hormoz Shams5, S Zahra Ghodsi4, Fereydoun Davatchi3.   

Abstract

OBJECTIVES: This study proposed to report the characteristics of paediatric Behçet's disease (PED-BD) in a cohort of patients from Iran's registry and compare them with different reports throughout the world.
METHODS: From a cohort of 7504 Iranian patients with Behçet's disease those diagnosed before the age of 16 years were included in this study. Data were collected on a standard protocol comprising 105 items, including demographic features, type of presentation, and different clinical and laboratory findings.
RESULTS: PED-BD was seen in 2.7% of patients. The male/female ratio was 1.02/1, and the mean age at onset was 10.5±3.4. Positive familial history was present in 9.9%. As a first manifestation, oral aphthosis was the most frequent (75%) followed by ocular lesions in 19.1%. The prevalence rates of various manifestations were as follows: oral aphthosis: 91.7%; genital ulcer: 42.2%; skin: 51.5% (pseudofolliculitis: 43.1%, erythema nodosum: 10.3%); ocular lesions: 66.2% (anterior uveitis 52%, posterior uveitis 58.3%, retinal vasculitis 39.7%); articular manifestations: 30.9%; neurological involvement: 4.9%; vascular involvement: 6.4% (venous 4.9%, arterial 2.5%); gastrointestinal manifestations: 5.9%; epididymo-orchitis: 8.7% (boys); high ESR (≥20): 50.8%; abnormal urine: 14.1%; positive pathergy test: 57%; HLA-B5/51: 48.7%. ICBD criteria have the highest sensitivity for the classification of PED-BD patients in Iran (91.7%).
CONCLUSIONS: The clinical spectrum of PED-BD in Iran in this study was similar to that of other reports; however, genital ulcers, skin lesions (notably erythema nodosum), and gastrointestinal involvement were noticed to occur less frequently, while ocular lesions were more frequent and more severe compared to other reports.

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Mesh:

Year:  2018        PMID: 29998839

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  6 in total

Review 1.  Pediatric Behçet's disease - clinical aspects and current concepts.

Authors:  Mehmet Yıldız; Oya Köker; Amra Adrovic; Sezgin Şahin; Kenan Barut; Özgür Kasapçopur
Journal:  Eur J Rheumatol       Date:  2019-09-05

2.  Performance of diagnostic criteria in pediatric Behçet's disease.

Authors:  Tuba Kurt; Fatma Aydın; Müge Sezer; P Nilüfer Tekgöz; Zahide Ekici Tekin; Elif Çelikel; Cüneyt Karagöl; Serkan Coşkun; Banu Acar
Journal:  Rheumatol Int       Date:  2021-01-15       Impact factor: 2.631

3.  Juvenile Behçet's disease: a tertiary center experience.

Authors:  Zahide Ekici Tekin; Elif Çelikel; Fatma Aydin; Tuba Kurt; Müge Sezer; Nilüfer Tekgöz; Cüneyt Karagöl; Serkan Coşkun; Melike Mehveş Kaplan; Banu Çelikel Acar
Journal:  Clin Rheumatol       Date:  2021-09-02       Impact factor: 2.980

Review 4.  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

Review 5.  Paediatric Behçet's Disease: A Comprehensive Review with an Emphasis on Monogenic Mimics.

Authors:  Ovgu Kul Cinar; Micol Romano; Ferhat Guzel; Paul A Brogan; Erkan Demirkaya
Journal:  J Clin Med       Date:  2022-02-26       Impact factor: 4.241

6.  Clinical profile and evolution of patients with juvenile-onset Behçet's syndrome over a 25-year period: insights from the AIDA network.

Authors:  Jurgen Sota; Donato Rigante; Giuseppe Lopalco; Giacomo Emmi; Stefano Gentileschi; Carla Gaggiano; Luisa Ciarcia; Virginia Berlengiero; Mariam Mourabi; Nicola Ricco; Sara Barneschi; Irene Mattioli; Gian Marco Tosi; Bruno Frediani; Maria Tarsia; Gerardo di Scala; Antonio Vitale; Florenzo Iannone; Claudia Fabiani; Luca Cantarini
Journal:  Intern Emerg Med       Date:  2021-04-09       Impact factor: 3.397

  6 in total

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