Behçet's disease - a difficult disease in terms of diagnosis in an adolescent patient

Authors

  • Helena Maria Ribeiro Fernandes General and Family Medicine, Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV
  • Maria Conceição Santos Silva Department of Pediatrics, Centro Hospitalar Póvoa de Varzim/Vila do Conde
  • Gabriela Amorim Casanova General and Family Medicine, Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV
  • Ana Catarina Andrade Peixoto General and Family Medicine, Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV

DOI:

https://doi.org/10.25753/BirthGrowthMJ.v26.i4.9959

Keywords:

Behçet’s disease, diagnosis, therapeutics

Abstract

Introduction: Behçet’s disease (BD) is a chronic multisystem disorder. The diagnosis is made only by using diagnostic criteria and children are rarely affected.
Case report: A 17-years-old adolescent with recurrent oral aphthous ulcers since 13 years of age, without any other symptoms. Differential diagnoses such as infections, hypovitaminosis, food allergy and celiac disease were excluded. In order to diagnose Behçet’s disease, the pathergy test was done and it was negative. At the age of 16, the adolescent developed facial papulopustules and acneiform nodules, undistinguishable from acne, and at 17 years of age, she developed a genital aphthous ulceration. The patient was sent to a pediatric rheumatology physician, and, considering a likely BD, started a treatment with oral colchicine, with reduction of the number and recurrence of oral aphthous ulcers. This patient has clinical criteria to be diagnosed with BD.
Discussion: This clinical report is a reminder of how important it is to continuously follow patients because of the insidious character of some diseases, including rheumatic, and highlights that BD can be hard to diagnosis in the paediatric population.

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Author Biographies

Helena Maria Ribeiro Fernandes, General and Family Medicine, Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV

Interna de Formação Específica de Medicina Geral e Familiar; Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV

Maria Conceição Santos Silva, Department of Pediatrics, Centro Hospitalar Póvoa de Varzim/Vila do Conde

Médica Especialista em Pediatria no Centro Hospitalar Póvoa de Varzim/Vila do Conde

Gabriela Amorim Casanova, General and Family Medicine, Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV

Médica Especialista em Medicina Geral e Familiar, Agrupamento dos Centros de Saúde Grande Porto IV, Póvoa de Varzim/Vila do Conde

Ana Catarina Andrade Peixoto, General and Family Medicine, Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV

Médica Interna na Unidade de Saúde Familiar do Mar, Agrupamento dos Centros de Saúde Grande Porto IV, Póvoa de Varzim/Vila do Conde

References

Borlu M, Ukşal Ü, Ferahbaş A, Evereklioglu C. Clinical features of Behçet’s disease in children. Int J Dermatol. 2006; 45:713-6.

Davatchi F, Shahram F, Chams-Davatchi C, Shams H, Nadji A, Akhlaghi M, et al. How to deal with Behcet’s disease in daily practice. Int J Rheum Dis. 2010; 13:105-16.

Neves FdS, Moraes JCBd, Gonçalves CR. Síndrome de Behçet: à procura de evidências. Rev Bras Reumatol. 2006; 46:21-9.

Piram M, Koné-Paut I. Maladie de Behçet de l’enfant. Rev Med Interne. 2014; 35:121-5.

Ozen S, Eroglu FK. Pediatric-onset Behçet disease. Curr Opin Rheumatol 2013; 25:636-42.

Koné-Paut I. Behçet’s disease in children, an overview. Pediatric Rheumatology 2016; 14:10.

Hatemi G, Silman A, Bang D, Bodaghi B, Chamberlain AM, Gul A, et al. EULAR recommendations for the management of Behçet disease. Ann Rheum Dis. 2008; 67:1656-62.

Comarmond C, Wechsler B, Cacoub P, Saadoun D. Traitement de la maladie de Behçet. Rev Med Interne. 2014; 35:126-38.

Yazici H, Yazici Y. Criteria for Behçet’s disease with reflections on all disease criteria. J Autoimmun. 2014; 48-49:104-7.

Published

2017-12-27

How to Cite

1.
Fernandes HMR, Silva MCS, Casanova GA, Peixoto ACA. Behçet’s disease - a difficult disease in terms of diagnosis in an adolescent patient. REVNEC [Internet]. 2017Dec.27 [cited 2024Mar.28];26(4):240-2. Available from: https://revistas.rcaap.pt/nascercrescer/article/view/9959

Issue

Section

Case Reports