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恒牙列中罕见牙本质发育异常与少牙畸形的同时发生:一例报告

Simultaneous occurrence of unusual odontodysplasia and oligodontia in the permanent dentition: report of a case.

作者信息

Fujiwara T, Nakano K, Sobue S, Ooshima T

机构信息

Department of Pedodontics, Osaka University Faculty of Dentistry, Japan.

出版信息

Int J Paediatr Dent. 2000 Dec;10(4):341-7. doi: 10.1046/j.1365-263x.2000.00217.x.

Abstract

Odontodysplasia is an uncommon clinicopathological condition with a variety of expressions. Although it is generally recognized as a localized disorder of dental tissue, its aetiology has not yet been well explained. In the present case, odontodysplasia with oligodontia in the permanent dentition is reported. The patient was in good health with normal stature and no other physical abnormalities. His parents and siblings were dentally and medically normal. The primary teeth appeared to be normal except for the primary second molars, where the enamel was malformed. However, the permanent incisors that had erupted into the oral cavity showed rough and hypoplastic enamel. An orthopantomogram showed 17 congenitally missing permanent teeth and malformation of the other 11 permanent teeth and tooth-germs. Because these findings were caused by developmental disturbances of both the mesodermal and ectodermal dental components, we diagnosed the present case as odontodysplasia accompanied by oligodontia in the permanent dentition.

摘要

牙发育异常是一种临床表现多样的罕见病。尽管它通常被认为是一种局限性的牙组织疾病,但其病因尚未得到很好的解释。在本病例中,报告了恒牙列中伴有少牙症的牙发育异常。患者身体健康,身材正常,无其他身体异常。他的父母和兄弟姐妹在牙齿和医学方面均正常。除了乳磨牙的釉质发育不良外,乳牙看起来正常。然而,萌出到口腔中的恒牙切牙显示釉质粗糙且发育不全。曲面断层片显示17颗恒牙先天缺失,另外11颗恒牙及牙胚发育畸形。由于这些表现是由牙中胚层和外胚层成分的发育障碍引起的,我们将本病例诊断为恒牙列少牙症伴牙发育异常。

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