Arhar Ana, Pavlič Alenka, Hočevar Luka
Department of Paediatric and Preventive Dentistry, Faculty of Medicine, University of Ljubljana, Vrazov trg 2, Ljubljana, Slovenia.
Department of Paediatric and Preventive Dentistry, University Medical Centre Ljubljana, Zaloška 2, Ljubljana, Slovenia.
BDJ Open. 2024 May 31;10(1):42. doi: 10.1038/s41405-024-00223-6.
Oral health is impaired in X-linked hypophosphatemia (XLH), resulting in delayed dental development, malocclusion, and radiographic abnormalities. This study investigates the oral manifestations in Slovenian XLH patients, focusing on enamel and dentin abnormalities and a literature review of spontaneous periapical abscesses in XLH cases.
To report XLH patients with specific oral signs and symptoms, histological analysis of affected teeth, and review of reported cases of XLH patients with spontaneous periapical abscesses.
Case reports: Seven XLH patients from the National Registry of Patients with Rare Diseases underwent a detailed oral examination, including X-ray reviews. The patients who were expected to have tooth exfoliation or extraction were asked to donate their teeth for histological analysis by scanning electron microscopy.
A literature search of four electronic databases and a manual bibliography search aimed to identify documented cases of XLH with periapical abscesses up to January 21, 2024. Inclusion criteria were confirmed XLH patients with periapical abscesses in English peer-reviewed publications.
Tooth samples from three XLH patients showed reduced dentin mineralisation, affecting one-third to one-half of the outer dentin. Inadequate mineralisation, uneven dentin tubules, and cracks and chipping in the enamel were observed, indicating mineralisation deviations. Similar cracks extended into the dentin and were also present in the root of the examined tooth. Based on the content of the 75 items identified in the search, spontaneous abscesses are not uncommon in patients with XLH.
XLH significantly affects patients' lives and requires lifelong treatment. Dental examinations consistently revealed oral problems, including malocclusion. Histological analysis confirmed structural changes, especially in the dentin. Despite continued treatment, XLH patients may have an increased risk of oral pathologies. Further research is needed to understand the impact of XLH and its treatment on dental health.
X连锁低磷血症(XLH)患者的口腔健康受损,导致牙齿发育延迟、咬合不正和影像学异常。本研究调查斯洛文尼亚XLH患者的口腔表现,重点关注釉质和牙本质异常,并对XLH病例中自发性根尖脓肿的文献进行综述。
报告有特定口腔体征和症状的XLH患者,对患牙进行组织学分析,并回顾报道的XLH患者自发性根尖脓肿病例。
病例报告:来自国家罕见病患者登记处的7名XLH患者接受了详细的口腔检查,包括X线检查。预计会有牙齿脱落或拔除的患者被要求捐赠牙齿,以便通过扫描电子显微镜进行组织学分析。
对四个电子数据库进行文献检索,并进行手动文献检索,旨在识别截至2024年1月21日有根尖脓肿的XLH病例记录。纳入标准为英文同行评审出版物中确诊的有根尖脓肿的XLH患者。
三名XLH患者的牙齿样本显示牙本质矿化减少,影响外层牙本质的三分之一至二分之一。观察到矿化不足、牙本质小管不均匀以及釉质中的裂纹和剥落,表明存在矿化偏差。类似的裂纹延伸到牙本质中,在所检查牙齿的根部也有出现。根据检索到的75篇文献的内容,自发性脓肿在XLH患者中并不罕见。
XLH严重影响患者生活,需要终身治疗。牙科检查一直发现口腔问题,包括咬合不正。组织学分析证实了结构变化,尤其是牙本质的变化。尽管持续治疗,但XLH患者口腔疾病的风险可能会增加。需要进一步研究以了解XLH及其治疗对牙齿健康的影响。