Department of Dermatology, Medical Faculty and Medical Center, University of Freiburg, Freiburg, Germany.
Special Care Dentistry Unit, Facultad de Odontologia, Universidad de Chile, Santiago, Chile.
JAMA Dermatol. 2024 May 1;160(5):544-549. doi: 10.1001/jamadermatol.2024.0065.
Kindler epidermolysis bullosa is a genetic skin-blistering disease associated with recessive inherited pathogenic variants in FERMT1, which encodes kindlin-1. Severe orofacial manifestations of Kindler epidermolysis bullosa, including early oral squamous cell carcinoma, have been reported.
To determine whether hypoplastic pitted amelogenesis imperfecta is a feature of Kindler epidermolysis bullosa.
DESIGN, SETTINGS, AND PARTICIPANTS: This longitudinal, 2-center cohort study was performed from 2003 to 2023 at the Epidermolysis Bullosa Centre, University of Freiburg, Germany, and the Special Care Dentistry Clinic, University of Chile in association with DEBRA Chile. Participants included a convenience sampling of all patients with a diagnosis of Kindler epidermolysis bullosa.
The primary outcomes were the presence of hypoplastic pitted amelogenesis imperfecta, intraoral wounds, gingivitis and periodontal disease, gingival hyperplasia, vestibular obliteration, cheilitis, angular cheilitis, chronic lip wounds, microstomia, and oral squamous cell carcinoma.
The cohort consisted of 36 patients (15 female [42%] and 21 male [58%]; mean age at first examination, 23 years [range, 2 weeks to 70 years]) with Kindler epidermolysis bullosa. The follow-up ranged from 1 to 24 years. The enamel structure was assessed in 11 patients, all of whom presented with enamel structure abnormalities. The severity of hypoplastic pitted amelogenesis imperfecta varied from generalized to localized pitting. Additional orofacial features observed include gingivitis and periodontal disease, which was present in 90% (27 of 30 patients) of those assessed, followed by intraoral lesions (16 of 22 patients [73%]), angular cheilitis (24 of 33 patients [73%]), cheilitis (22 of 34 patients [65%]), gingival overgrowth (17 of 26 patients [65%]), microstomia (14 of 25 patients [56%]), and vestibular obliteration (8 of 16 patients [50%]). Other features included chronic lip ulcers (2 patients) and oral squamous cell carcinoma with lethal outcome (2 patients).
These findings suggest that hypoplastic pitted amelogenesis imperfecta is a feature of Kindler epidermolysis bullosa and underscore the extent and severity of oral manifestations in Kindler epidermolysis bullosa and the need for early and sustained dental care.
Kindler 型大疱性表皮松解症是一种遗传性皮肤水疱病,与 FERMT1 中的隐性遗传致病性变异有关,FERMT1 编码 kindlin-1。已报道 Kindler 型大疱性表皮松解症严重的口腔表现,包括早期口腔鳞状细胞癌。
确定先天性釉质不全伴牙釉质小凹是否为 Kindler 型大疱性表皮松解症的特征。
设计、地点和参与者:这项 2003 年至 2023 年在德国弗赖堡大学的大疱性表皮松解症中心和智利大学的特殊护理牙科诊所进行的纵向、2 中心队列研究,与智利的 DEBRA 合作进行。参与者包括所有确诊为 Kindler 型大疱性表皮松解症的患者的方便抽样。
主要结局是存在先天性釉质不全伴牙釉质小凹、口腔内伤口、牙龈炎和牙周病、牙龈增生、前庭闭塞、唇炎、口角炎、慢性唇溃疡、小口畸形和口腔鳞状细胞癌。
该队列包括 36 名患者(15 名女性[42%]和 21 名男性[58%];首次检查时的平均年龄为 23 岁[范围:2 周至 70 岁]),患有 Kindler 型大疱性表皮松解症。随访时间从 1 年到 24 年不等。11 名患者评估了牙釉质结构,他们均表现出牙釉质结构异常。先天性釉质不全伴牙釉质小凹的严重程度从全身性小凹到局限性小凹不等。观察到的其他口腔特征包括牙龈炎和牙周病,在评估的 30 名患者中有 90%(27 名)存在,其次是口腔内病变(22 名患者中的 16 名[73%])、口角炎(33 名患者中的 24 名[73%])、唇炎(34 名患者中的 22 名[65%])、牙龈增生(26 名患者中的 17 名[65%])、小口畸形(25 名患者中的 14 名[56%])和前庭闭塞(16 名患者中的 8 名[50%])。其他特征包括慢性唇溃疡(2 例)和致命性口腔鳞状细胞癌(2 例)。
这些发现表明先天性釉质不全伴牙釉质小凹是 Kindler 型大疱性表皮松解症的特征,并强调了 Kindler 型大疱性表皮松解症口腔表现的程度和严重性,以及早期和持续的口腔护理的必要性。