Cascone P, Rivaroli A, Vetrano S
Department of Maxillofacial Surgery, University of Rome La Sapienza, Italy.
J Craniofac Surg. 1998 Sep;9(5):472-6.
The authors focus on a case of scleroderma, or progressive systemic sclerosis. Scleroderma is a disease of unknown cause, characterized by an abnormal synthesis of connective tissues that causes a sclerosis of the skin involving organs and systems at various levels. It may appear in different forms and may involve, although not frequently, the maxillofacial district. The authors examined a 21-year-old woman who had been diagnosed with systemic progressive sclerosis in 1994. The patient showed a strong limitation of oral aperture, evidenced by an electrognathographic test, and osseous changes. Panoramic and full-mouth intraoral radiographs showed a complete agenesis of coronoid processes on both sides, whereas the angles and the rising branches of the mandibular and periodontal ligaments appeared normal. The patient was diagnosed as having maxillofacial localization of scleroderma with involvement of coronoid processes bilaterally.
作者聚焦于一例硬皮病,即进行性系统性硬化症。硬皮病是一种病因不明的疾病,其特征是结缔组织异常合成,导致皮肤硬化,累及不同层面的器官和系统。它可能以不同形式出现,虽不常见,但可能累及颌面区域。作者检查了一名21岁女性,她于1994年被诊断为系统性进行性硬化症。患者表现出明显的张口受限,经颌电图测试证实,且存在骨质改变。全景片和全口牙片显示双侧喙突完全缺如,而下颌角、升支及牙周韧带看起来正常。该患者被诊断为硬皮病颌面局部病变,双侧喙突受累。