Dulla Joëlle A, Meyer-Lueckel Hendrik
Department of Restorative, Preventive, and Pediatric Dentistry, School of Dental Medicine, University of Bern, Switzerland.
Swiss Dent J. 2021 Mar 25;131(11). doi: 10.61872/sdj-2021-11-763.
Molar-incisor hypomineralisation (MIH) is clinically defined as demarcated structural enamel defects affecting at least one first permanent molar with or without the involvement of incisors. It is foremost a qualitative developmental defect of systemic origin. The prevalence for MIH is estimated at 12.9% with significant differences between countries. Its etiology and pathogenesis are still not completely understood. Several environmental and medical causes have been suggested to alter enamel maturation. The hypomineralised enamel may collapse shortly after eruption and as a consequence caries lesions seem more likely to develop. Besides cavitation, hypersensitivity and/or pain are the hallmarks of clinical symptoms. Both are associated with increased dental anxiety and fear of children suffering from MIH. Consequently, patients' care and management are challenging and necessitates a large range of non-, micro- and invasive strategies. MIH might be mixed up with three different other types of developmental defects in the enamel: fluorosis, enamel hypoplasia, and amelogenesis imperfecta. Careful diagnostic differentiation should be made before starting any dental treatment. A recent published classification system links the severity of the lesion to a treatment need index. This index is based on four values regarding two key symptoms: hypersensitivity and post-eruptiv enamel breakdown (PEB). Without PEB sealing is strongly recommended in order to prevent caries. For hypersensitive teeth as well as those with PEB use of glass ionomer cement as an intermediate cover, but mainly composite resins are materials of choice. For improvement of aesthetically compromised MIH-incisors, the resin infiltration technique has been proposed.
磨牙-切牙矿化不全(MIH)在临床上被定义为界限分明的釉质结构缺陷,累及至少一颗第一恒磨牙,可伴有或不伴有切牙受累。它首先是一种全身性起源的定性发育缺陷。MIH的患病率估计为12.9%,各国之间存在显著差异。其病因和发病机制仍未完全明确。已提出多种环境和医学原因可改变釉质成熟。矿化不全的釉质在萌出后不久可能会崩解,因此龋齿病变似乎更易发生。除了形成空洞外,牙齿敏感和/或疼痛是临床症状的标志。这两者都与患有MIH的儿童牙齿焦虑和恐惧增加有关。因此,患者的护理和管理具有挑战性,需要一系列非侵入性、微侵入性和侵入性策略。MIH可能会与釉质中另外三种不同类型的发育缺陷混淆:氟斑牙、釉质发育不全和牙釉质形成不全。在开始任何牙科治疗之前,应进行仔细的诊断鉴别。最近发布的一种分类系统将病变的严重程度与治疗需求指数相关联。该指数基于关于两个关键症状的四个值:牙齿敏感和萌出后釉质崩解(PEB)。对于无PEB的情况,强烈建议进行封闭以预防龋齿。对于敏感牙齿以及有PEB的牙齿,使用玻璃离子水门汀作为中间覆盖材料,但主要选择复合树脂材料。为了改善美观受损的MIH切牙,已提出树脂渗透技术。