Juvenile Behçet syndrome: a contemporary view and differential diagnosis in pediatric practice DOI
Mehmet Yıldız, Oya Köker, Özgür Kasapçopur

et al.

Current Opinion in Rheumatology, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 18, 2024

Purpose of review This aims to provide a comprehensive and contemporary overview juvenile Behçet syndrome (jBS), highlighting its clinical manifestations, diagnostic challenges, treatment strategies. Recent findings syndrome, with intricate etiopathogenesis diverse phenotypes, is more aptly classified as than single disease. Its heterogeneous nature requires broad approach sophisticated differential diagnosis capabilities. The relatively rare occurrence combined incomplete presentations overlapping diagnoses, presents significant particularly in pediatric cases. Nevertheless, substantial progress has been made treatment, especially managing inflammatory components preventing complications. Juvenile patients, given their developmental stage, require distinct therapeutic strategies compared adults, careful consideration side effects on growth psychosocial development. Summary To ensure early identification jBS, it imperative refine develop criteria specifically tailored populations. With deeper understanding the disease mechanisms, protocols should be designed address developmental, psychosocial, individual needs aiming minimize long-term effects. Additionally, studies considering age, sex, ethnic differences are necessary fill gaps literature resolve existing inconsistencies.

Language: Английский

Juvenile Behçet syndrome: a contemporary view and differential diagnosis in pediatric practice DOI
Mehmet Yıldız, Oya Köker, Özgür Kasapçopur

et al.

Current Opinion in Rheumatology, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 18, 2024

Purpose of review This aims to provide a comprehensive and contemporary overview juvenile Behçet syndrome (jBS), highlighting its clinical manifestations, diagnostic challenges, treatment strategies. Recent findings syndrome, with intricate etiopathogenesis diverse phenotypes, is more aptly classified as than single disease. Its heterogeneous nature requires broad approach sophisticated differential diagnosis capabilities. The relatively rare occurrence combined incomplete presentations overlapping diagnoses, presents significant particularly in pediatric cases. Nevertheless, substantial progress has been made treatment, especially managing inflammatory components preventing complications. Juvenile patients, given their developmental stage, require distinct therapeutic strategies compared adults, careful consideration side effects on growth psychosocial development. Summary To ensure early identification jBS, it imperative refine develop criteria specifically tailored populations. With deeper understanding the disease mechanisms, protocols should be designed address developmental, psychosocial, individual needs aiming minimize long-term effects. Additionally, studies considering age, sex, ethnic differences are necessary fill gaps literature resolve existing inconsistencies.

Language: Английский

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