Soares Alvaro Cavalheiro, Pires Fabio Ramoa, de Oliveira Quintanilha Nara Regina, Santos Lilian Rocha, Amin Dick Thaylla Nunez, Dziedzic Arkadiusz, Picciani Bruna Lavinas Sayed
Postgraduate Program in Dentistry, Nova Friburgo Health Institute, Fluminense Federal University, Nova Friburgo 28625-650, Brazil.
Department of Oral Pathology, School of Dentistry, Rio de Janeiro State University, Rio de Janeiro 20551-030, Brazil.
Biomedicines. 2023 Jul 3;11(7):1882. doi: 10.3390/biomedicines11071882.
Behçet's disease (BD) is a rare chronic auto-inflammatory systemic disease with non-specific oral manifestations, categorised as generalised variable vessel vasculitis that requires an interdisciplinary approach to diagnose due to its phenotypic heterogeneity. Whilst the oral lesions that reoccur in BD underpin the complex diagnostic process, the crucial role of dental professionals is highlighted in a case report summarised herein. We present a case of a 47-year-old male referred to the Oral Medicine Department by a rheumatologist after previous hospitalization for thrombosis of the iliac vein and inferior vena cava. He had elevated inflammatory C-reactive protein biomarker and an increased erythrocyte sedimentation rate. Recurrent episodes of folliculitis, oral and genital ulcers were reported. Clinical examination revealed multiple ulcerations in the oral mucosa. The complementary, histopathological analysis performed to rule out other disorders, based on excisional biopsy, showed non-keratinised stratified squamous epithelium with areas of exocytosis and ulceration. The connective tissue presented an intense mixed inflammatory infiltrate, congested blood vessels, haemorrhage, vasculitis, and HLA-B genotyping identified the expression of HLA-B15, further supporting the BD diagnosis. Treatment was initiated with colchicine, prednisolone, and weekly subcutaneous administration of methotrexate and resulted in the complete remission of oral lesions and no recurrence of other manifestations.
This BD case report emphasizes the importance of a multidisciplinary approach in diagnosing BD, including the use of histopathological assessment and genetic profiling. It highlights the significance of thorough intraoral assessment and referral to a multidisciplinary team for diagnosis. The oral manifestations of BD as the primary symptoms often indicate underlying major systemic pathologies. The authors stress the need for a structured diagnostic algorithm to facilitate timely and effective management of BD.
白塞病(BD)是一种罕见的慢性自身炎症性全身性疾病,具有非特异性口腔表现,归类为全身性可变血管炎,由于其表型异质性,需要采用多学科方法进行诊断。虽然BD中反复出现的口腔病变是复杂诊断过程的基础,但本文总结的一例病例报告突出了牙科专业人员的关键作用。我们报告一例47岁男性病例,该患者此前因髂静脉和下腔静脉血栓形成住院,后由风湿病学家转诊至口腔医学科。他的炎症生物标志物C反应蛋白升高,红细胞沉降率增加。报告有复发性毛囊炎、口腔和生殖器溃疡。临床检查发现口腔黏膜有多处溃疡。基于切除活检进行的补充组织病理学分析以排除其他疾病,结果显示为非角化复层鳞状上皮,伴有外渗和溃疡区域。结缔组织呈现强烈的混合性炎症浸润、血管充血、出血、血管炎,HLA - B基因分型鉴定出HLA - B15的表达,进一步支持BD的诊断。开始使用秋水仙碱、泼尼松龙治疗,并每周皮下注射甲氨蝶呤,结果口腔病变完全缓解,其他表现未复发。
本BD病例报告强调了多学科方法在诊断BD中的重要性,包括使用组织病理学评估和基因分析。它突出了全面口腔内评估以及转诊至多学科团队进行诊断的重要性。BD的口腔表现作为主要症状往往提示潜在的重大全身性疾病。作者强调需要一种结构化的诊断算法,以促进BD的及时有效管理。