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Accès ouvert déclaré 2025 article

Case Report of Behçet's Syndrome with Significant Oral Manifestations

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Résumé fourni par la source

Aims: This report presents a clinical case of an 11-year-old female patient diagnosed with Behçet's Syndrome, who was diagnosed and treated at a private hospital in the southern region of the country. Case report: An 11-year-old girl who arrived at the emergency exhibited oral mucosal lesions, ocular discharge, throat pain, and persistent leukorrhea. On physical examination, the patient had no visible skin lesions. Patient presents with sialorrhea and ulcerated genital lesions. Both eyes exhibited bilateral mucoid discharge. The labial mucosa and lips showed multiple ulcers and erosions, which were also present on the palate, posterior region, back, and edges of the tongue. Vulvar hygiene, urethral probing, application of topical anti-inflammatory to the region, and chamomile tea were administered. Five daily photobiomodulation sessions were carried out with low-power laser for lesions of the oral cavity and oropharynx, in addition to oral hygiene guidance, use of 0.12% chlorhexidine for oral hygiene, chamomile tea, chamomile-based ointment and anesthetic spray. 5 laser sessions were performed due to the cost of treatment, after 5 days the patient was discharged and complete remission was not monitored. Conclusion: Despite being a challenging condition, BS is relatively common and demands accurate diagnosis and effective management.

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Contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Case Report of Behçet's Syndrome with Significant Oral Manifestations
Date Crossref
03/02/2025
Éditeur
Anima Educação
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude et ne compte pas comme une seconde source scientifique indépendante.

Institutions déclarées

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Sujets associés

Ocular Diseases and Behçet’s SyndromeOtitis Media and Relapsing PolychondritisIgG4-Related and Inflammatory Diseases

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