Watanabe K
Department of Periodontics, College of Dentistry, University of Illinois, Chicago.
J Periodontal Res. 1990 Jan;25(1):31-48. doi: 10.1111/j.1600-0765.1990.tb01205.x.
This paper reviews the literature on prepubertal periodontitis (PP) according to the definition and the classification of PP by Page. The generalized form of PP (G-PP) defined by Page was identified as the oral manifestation of a systemic disease called leukocyte adhesion deficiency (LAD) and thus the pathogenesis is known at the molecular level. On the other hand, the localized form of PP (L-PP) is a disease defined by clinical criteria and its pathogenesis is not known at the molecular level. The reported prevalence of L-PP differs widely in reports, according to the methodology and population studied. However, it seems to be at least 0.84% or greater. Potential periodontal pathogens that have been associated with L-PP include the following bacteria: Actinobacillus actinomycetemcomitans (A.a.), Bacteroides intermedius, Bacteroides gingivalis, Capnocytophaga sputigena, and Eikenella corrodens. Suggested contributing factors have included PMN or monocyte chemotactic defects and cementum defects. There is no unique pattern of bone loss in L-PP; however, there may be a type of periodontitis that affects all deciduous teeth, in the absence of LAD. L-PP may lead to localized juvenile periodontitis (LJP) or generalized juvenile periodontitis (GJP). Histiocytosis X, hypophosphatasia and mild forms of blood dyscrasias may have minimal or no clinical signs and symptoms except for alveolar bone loss. Therefore diseases known to be associated with alveolar bone loss must be definitively excluded in prepubertal children until the pathogenesis of L-PP at the cellular and molecular levels is understood and L-PP can be definitively diagnosed either as a distinct disease entity or entities.
本文根据佩奇对青春期前牙周炎(PP)的定义和分类对相关文献进行综述。佩奇定义的广泛性青春期前牙周炎(G-PP)被确定为一种名为白细胞黏附缺陷(LAD)的全身性疾病的口腔表现,因此其发病机制在分子水平上是已知的。另一方面,局限性青春期前牙周炎(L-PP)是一种根据临床标准定义的疾病,其发病机制在分子水平上尚不清楚。根据所研究的方法和人群,报告的L-PP患病率在不同报告中有很大差异。然而,其似乎至少为0.84%或更高。与L-PP相关的潜在牙周病原体包括以下细菌:伴放线放线杆菌(A.a.)、中间普氏菌、牙龈普氏菌、嗜二氧化碳噬纤维菌和腐蚀埃肯菌。提示的促成因素包括中性粒细胞或单核细胞趋化缺陷以及牙骨质缺陷。L-PP中不存在独特的骨丧失模式;然而,在不存在LAD的情况下,可能存在一种影响所有乳牙的牙周炎类型。L-PP可能导致局限性青少年牙周炎(LJP)或广泛性青少年牙周炎(GJP)。组织细胞增多症X、低磷酸酯酶症和轻度血液恶液质除牙槽骨丧失外可能几乎没有或没有临床体征和症状。因此,在青春期前儿童中,必须明确排除已知与牙槽骨丧失相关的疾病,直到在细胞和分子水平上了解L-PP的发病机制,并且L-PP能够被明确诊断为一种或多种不同的疾病实体。