Suppr超能文献

单侧冠状突增生与面部不对称的早期手术治疗

Early surgical treatment in unilateral coronoid hyperplasia and facial asymmetry.

作者信息

Galiè Manlio, Consorti Giuseppe, Tieghi Riccardo, Denes Stefano Andrea, Fainardi Enrico, Schmid Judith Louisa, Neuschl Matthias, Clauser Luigi

机构信息

Unit of Cranio Maxillo Facial Surgery, Centre for Craniofacial Deformities and Orbital Surgery, Hospital and University St Anna, Ferrara, Italy.

出版信息

J Craniofac Surg. 2010 Jan;21(1):129-33. doi: 10.1097/SCS.0b013e3181c46a30.

Abstract

Unilateral coronoid hyperplasia is a rare condition in the pediatric age. It may be an unrecognized cause of restricted mouth opening in children.The limited jaw movement is due to the enlargement of the coronoid process of the mandible that impinges on the zygomatic arch during mouth opening. This pathologic condition is still unknown and often misdiagnosed.Although in the past the term osteochondroma has been used to describe most of the unilateral and a few of the bilateral cases, there is no histologic evidence that the process has a neoplastic origin.Microscopic examination of the removed coronoid process has revealed hyperplastic compact bone covered with a thin layer of normal cartilage.There are multiple causes of mandibular hypomobility, each of them associated with different anatomic structures and etiologies, and a large number of cases, mostly bilateral, are idiopathic in nature.Several theories of pathogenesis have been proposed: temporomandibular joint dysfunctions, mandibular hypomobility, temporalis hyperactivity, hormonal stimulus, persistent cartilage growth center, genetic inheritance, and family factors.Unilateral coronoid hyperplasia is usually due to a trauma or a pathologic condition and is associated with facial asymmetry, being more frequently seen in women with histologic chondromatous or neoplastic changes. A thorough clinical history should include information about the onset and progression of pain and other subjective symptoms.In this study, we present a case of unilateral hyperplasia of the coronoid process in a 3 year-old female who, to the best of our knowledge, is the youngest patient so far reported with such anomaly.Our findings support the recommendation that early surgical treatment and aggressive postoperative physical therapy should be taken into account to allow for recovery of morphology and growth function in children.

摘要

单侧冠状突增生在儿童期是一种罕见的病症。它可能是儿童张口受限未被认识到的原因。下颌运动受限是由于下颌冠状突增大,在张口时撞击颧弓所致。这种病理状况仍不为人所知,且常被误诊。尽管过去曾用骨软骨瘤这一术语来描述大多数单侧及少数双侧病例,但并无组织学证据表明该病变起源于肿瘤。对切除的冠状突进行显微镜检查发现,其为增生的致密骨,表面覆盖一层薄的正常软骨。下颌运动障碍有多种原因,每种原因都与不同的解剖结构和病因相关,而且大量病例(大多为双侧)本质上是特发性的。已经提出了几种发病机制理论:颞下颌关节功能障碍、下颌运动障碍、颞肌亢进、激素刺激、持续的软骨生长中心、遗传遗传和家族因素。单侧冠状突增生通常由创伤或病理状况引起,与面部不对称有关,在有组织学软骨瘤样或肿瘤性改变的女性中更常见。详尽的临床病史应包括疼痛及其他主观症状的发作和进展情况等信息。在本研究中,我们报告了一例3岁女性单侧冠状突增生的病例,据我们所知,这是迄今报道的患有此类异常的最年轻患者。我们的研究结果支持这样的建议,即应考虑早期手术治疗及积极的术后物理治疗,以使儿童恢复形态和生长功能。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验