Lee Jang-Jaer, Hung Hsin-Chia, Cheng Shi-Jung, Chen Yi-Jane, Chiang Chun-Pin, Liu Bu-Yuan, Jeng Jiiang-Huei, Chang Hao-Hueng, Kuo Ying-Shiung, Lan Wan-Hong, Kok Sang-Heng
School of Dentistry, National Taiwan University College of Medicine, Taipei, Taiwan.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Apr;101(4):472-80. doi: 10.1016/j.tripleo.2005.07.024. Epub 2006 Jan 19.
The issue of existence of malignancy within oral leukoplakia has seldom been addressed in Taiwan. The aims of this study were to investigate the prevalence of carcinoma and dysplasia within oral leukoplakia at the time of clinical diagnosis and to identify the associated risk factors in Taiwan.
The prevalence rate of malignancy and dysplasia in 1046 oral leukoplakias at a university hospital was calculated. Univariate and multivariate analyses by the Mantel-Haenszel method and multiple logistic regression model were performed to examine risk factors associated with the presence of carcinoma and dysplasia within the lesions.
The prevalence rate of carcinoma was 12.9%. The relative risks for the presence of malignancy in leukoplakias on the tongue/floor of mouth and with nonhomogeneous appearance were 2.72- and 28.13-fold by multivariate logistic regression analysis, when compared with those on buccal mucosa and lesions having homogeneous surface (both P < .05). In contrast, patients who both smoked and chewed betel quid had a significantly lower risk for carcinoma than the abstainers (P < .05). A synergistic effect between the 2 major risk factors of clinical appearance and lesion site was evident. Nonhomogeneous leukoplakia on tongue/floor of mouth had a 43.10-fold higher risk compared to homogeneous lesions located on buccal mucosa or other sites (P < .05). However, homogeneous leukoplakia in buccal mucosa or other sites of the oral cavity still had the possibility of having carcinoma within the lesion. The prevalence of dysplasia was 45.6% among the noncancerous leukoplakias with risk factors similar to those for carcinoma.
Our results demonstrate that some leukoplakias contain a malignant component. Lesions with certain features are more prone to carcinoma, but no clinical attributes can bring certitude. Therefore, all oral leukoplakias should be submitted to microscopic analysis before any definite treatment or long-term follow-up.
台湾地区很少探讨口腔白斑内恶性病变的存在问题。本研究的目的是调查临床诊断时口腔白斑内癌和发育异常的患病率,并确定台湾地区相关的危险因素。
计算某大学医院1046例口腔白斑中恶性病变和发育异常的患病率。采用Mantel-Haenszel法和多元逻辑回归模型进行单因素和多因素分析,以检查与病变内癌和发育异常存在相关的危险因素。
癌的患病率为12.9%。多因素逻辑回归分析显示,与颊黏膜白斑及表面均匀的病变相比,舌/口底白斑及外观不均匀的白斑发生恶性病变的相对风险分别为2.72倍和28.13倍(均P <.05)。相比之下,既吸烟又嚼槟榔的患者患癌风险明显低于不吸烟者(P <.05)。临床外观和病变部位这两个主要危险因素之间存在协同作用。舌/口底的不均匀性白斑与颊黏膜或其他部位的均匀性病变相比,发生恶性病变的风险高43.10倍(P <.05)。然而,颊黏膜或口腔其他部位的均匀性白斑病变内仍有可能存在癌。在具有与癌相似危险因素的非癌性白斑中,发育异常的患病率为45.6%。
我们的结果表明,一些白斑含有恶性成分。具有某些特征的病变更容易发生癌变,但没有任何临床特征能够确诊。因此,在进行任何明确的治疗或长期随访之前,所有口腔白斑均应进行显微镜检查。