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硬皮病和系统性硬化症的颌面影响:病例报告及文献综述

Maxillofacial Implications of Scleroderma and Systemic Sclerosis: A Case Report and Literature Review.

作者信息

Burchfield Charles, Vorrasi John

机构信息

Chief Resident, Department of Oral and Maxillofacial Surgery, University of Rochester Medical Center, Eastman Institute for Oral Health, Rochester, NY.

Assistant Professor and Associate Program Director, Department of Oral and Maxillofacial Surgery, University of Rochester Medical Center, Eastman Institute for Oral Health, Rochester, NY.

出版信息

J Oral Maxillofac Surg. 2019 Jun;77(6):1203-1208. doi: 10.1016/j.joms.2019.01.027. Epub 2019 Jan 28.

Abstract

Scleroderma and more generally systemic sclerosis comprise a group of autoimmune diseases characterized by increased collagen synthesis and deposition within connective tissue. The Scleroderma Foundation estimates that as many as 300,000 persons in the United States have scleroderma. Although the etiology of the disease is unknown, it is thought to be related to chronic inflammation secondary to autoimmune tissue damage. Scleroderma has variable presentations and may result in changes to the skin, blood vessels, muscles, and internal organs. Oral and maxillofacial findings can include limited mouth opening; xerostomia; periodontal disease; widening of the periodontal ligament space; zygomatic arch resorption; and resorption of the mandibular angle, coronoid process, and condyle. We present the case of a 26-year-old female patient with scleroderma who exhibited extreme maxillofacial manifestations of the disease.

摘要

硬皮病,更广义地说系统性硬化症,是一组自身免疫性疾病,其特征是结缔组织内胶原蛋白合成和沉积增加。硬皮病基金会估计,美国有多达30万人患有硬皮病。尽管该病的病因尚不清楚,但据认为与自身免疫性组织损伤继发的慢性炎症有关。硬皮病有多种表现形式,可能导致皮肤、血管、肌肉和内脏发生变化。口腔颌面部表现可包括张口受限、口干、牙周病、牙周膜间隙增宽、颧弓吸收以及下颌角、冠突和髁突吸收。我们报告一例26岁患有硬皮病的女性患者,该患者表现出该病极端的颌面部表现。

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