Behçet's disease: a narrative review

Authors

  • Thiago José Islanderson dos Santos Castro UNINASSAU
  • Josiane Simplicio de Abreu UNINASSAU
  • João Pedro Gomes Pequeno Gonzaga UNINASSAU
  • Rômulo José Falcão Farias UNINASSAU
  • Brenda Lorenna de Jesus Araújo UniAtenas
  • Beatriz Bastos Santos UNINASSAU
  • Maria Gabriela Lermen de Souza UNINASSAU
  • Liz Silva Mariano UNINASSAU
  • Pedro Lucas Pessoa Cardoso UNINASSAU
  • Gabriel Alves Da Silva Santiago UNINASSAU
  • Ana Caroline dos Santos Sousa UNINASSAU
  • Camila Camaia Souza Winter UNINASSAU
  • Caio Gabriel Ferreira Souza UNINASSAU
  • Gabriela Castro de França UNINASSAU
  • Brenna Martins Barboza UNINASSAU
  • Emanoele Batista Rafael
  • Henrique Lima Martins
  • Monique Lima Martins

DOI:

https://doi.org/10.36557/2674-8169.2025v7n6p480-492

Keywords:

Behcet Syndrome, Vasculitis, Oral Ulcer, Erythema Nodosum, Autoimmunity

Abstract

This article aims to explore the pathophysiology, clinical manifestations, and therapeutic options of Behçet's Disease (BD) based on recent scientific publications. Studies published between 2019 and 2024, in English and Portuguese, were selected from the PubMed database, using terms related to the disease. BD is a chronic inflammatory vasculitis of autoimmune origin, which can affect vessels of different calibers and compromise multiple systems of the body. Its main manifestations include recurrent oral and genital ulcers, skin lesions, joint involvement, and gastrointestinal and neurological symptoms. Among the most serious complications, uveitis stands out, which can progress to irreversible visual loss. The diagnosis is essentially clinical and follows the criteria of the International Study Group for Behçet's Disease, based on the recurrence of manifestations. Although there is no cure, treatment aims to control inflammation and reduce the risk of complications, with immunosuppressants and anti-inflammatories being the main therapeutic approaches. Early diagnosis and ongoing medical monitoring are essential to improve the prognosis and quality of life of patients.

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References

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Published

2025-06-08

How to Cite

Castro, T. J. I. dos S., Abreu , J. S. de, Gonzaga, J. P. G. P., Farias, R. J. F., Araújo, B. L. de J., Santos , B. B., Souza , M. G. L. de, Mariano , L. S., Cardoso , P. L. P., Santiago , G. A. D. S., Sousa , A. C. dos S., Winter , C. C. S., Souza , C. G. F., França , G. C. de, Barboza , B. M., Rafael, E. B., Martins, H. L., & Martins, M. L. (2025). Behçet’s disease: a narrative review . Brazilian Journal of Implantology and Health Sciences, 7(6), 480–492. https://doi.org/10.36557/2674-8169.2025v7n6p480-492