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Diagnosis of childhood-oncet Behcet’s disease: a case report

https://doi.org/10.18705/2782-3806-2022-2-5-85-89

Abstract

Behcet disease is autoimmune vasculitis with predominantly mucocutaneous manifestations; eye, gastrointestinal and nervous system involvement is also possible. Behcet disease is relatively rare in pediatric population.
This article presents the case of Behcet’s disease in a 17-year-old boy, with a usual delay in the diagnosis, the absence of internal organs involvement and successful first-line therapy (colchicine).

About the Authors

E. M. Kuchinskaya
Almazov National Medical Research Centre
Russian Federation

Ph.D. of Medical Sciences, rheumatologist in outpatient department for children



A. M. Nikonenko
Almazov National Medical Research Centre
Russian Federation

head of outpatient department for children



References

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3. Koné-Paut I, Shahram F, Darce-Bello M, et al. Consensus classification criteria for paediatric Behçet’s disease from a prospective observational cohort: PEDBD. Ann Rheum Dis. 2016; 75: 958–64.

4. Hatemi G, Christensen R, Bang D, et al. 2018 update of the EULAR recommendations for the management of Behçet’s syndrome. Ann Rheum Dis. 2018; 77: 808–18.

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6. Arida A, Fragiadaki K, Giavri E, et al. Anti-TNF agents for Behçet’s disease: analysis of published data on 369 patients. Sem Arthr Rheum. 2011; 41:61–70.


Review

For citations:


Kuchinskaya E.M., Nikonenko A.M. Diagnosis of childhood-oncet Behcet’s disease: a case report. Russian Journal for Personalized Medicine. 2022;2(5):85-89. (In Russ.) https://doi.org/10.18705/2782-3806-2022-2-5-85-89

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ISSN 2782-3806 (Print)
ISSN 2782-3814 (Online)