Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Erciyes University, Kayseri, Turkey.
Aust Dent J. 2011 Dec;56(4):433-6. doi: 10.1111/j.1834-7819.2011.01372.x.
Langerhans' cell histiocytosis (LCH) is a rare disease where different organs and systems may be affected. Oral involvement generally consists of mucosal ulceration associated with lesions of the underlying bone. Many reports exist about the misdiagnosis of this disease. Various symptoms may lead the clinician to an incorrect diagnosis, especially with multiple organ involvement. Oral manifestations are common, and dentists should be aware of this disease and evaluate intraoral findings accordingly. This study presents an LCH case characterized by oral mucosal ulcerations with no involvement of the underlying bone. A definitive diagnosis was made by open biopsy from the oral mucosa.
朗格汉斯细胞组织细胞增生症(LCH)是一种罕见疾病,可能会影响不同的器官和系统。口腔受累通常表现为黏膜溃疡,伴有骨下病变。关于这种疾病的误诊有很多报道。各种症状可能导致临床医生做出错误的诊断,特别是在多个器官受累的情况下。口腔表现较为常见,牙医应该对此病有所了解,并相应地评估口腔内的发现。本研究报告了一例以口腔黏膜溃疡为特征、无骨下受累的 LCH 病例。通过口腔黏膜开放性活组织检查做出明确诊断。