特殊患者:大疱性表皮松解症

R. Elias
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引用次数: 0

摘要

背景:大疱性表皮松解症(EB)是一种相对罕见的遗传性皮肤病,具有不同的临床表现,其特征是皮肤和粘膜上出现水泡。某些形式的EB表现为口腔疾病,如上颚水泡、舌运动困难、口腔底部、嘴唇疤痕,此外还有牙齿发育不良、显微切除术和牙周病。病例描述:在本工作中,作者回顾了有关该主题的文献,并提出了一例15岁隐性营养不良大疱性表皮松解症患者的临床病例,重点关注该疾病的主要口腔表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Special Patients: Epidermolysis Bullosa
Background: Epidermolysis bullosa (EB) is a relatively rare hereditary dermatosis that has different clinical presentations and is characterized by the appearance of blisters on the skin and mucous membranes. Some forms of EB present stomatological manifestations, such as blisters on the palate, motor difficulties of the tongue, floor of the mouth, scars on the lips, in addition to dental dysplasias, microstomia and periodontal disease. Case description: In the present work, the author reviews the literature on the subject and present a clinical case of a 15-year-old patient with recessive dystrophic epidermolysis bullosa, focusing on the main stomatological manifestations of the disease.
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