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先天性无痛症患者的张口受限和口腔病变的正畸治疗和管理:病例报告。

Orthodontic treatment and management of limited mouth opening and oral lesions in a patient with congenital insensitivity to pain: case report.

机构信息

Department of Dental, Oral and Maxillo-Facial Sciences, University of Catanzaro Magna Graecia, Italy.

出版信息

J Oral Rehabil. 2009 Jan;36(1):71-8. doi: 10.1111/j.1365-2842.2008.01887.x. Epub 2008 Oct 22.

Abstract

Congenital insensitivity to pain is a rare clinical syndrome characterized by dramatic impairment of pain perception since birth and is generally caused by a hereditary sensory and autonomic neuropathy with loss of the small-calibre, nociceptive nerve fibres. We report a 9-year-old case, with a generalized congenital insensitivity to pain. The patient was referred to our Department by a private orthodontist for severe limited mouth opening and multiple oral ulcers which greatly worsened after starting the orthodontic treatment. The management of his oral lesions of the limited mouth opening and of the orthodontic treatment are described. The management approach aimed to improve mandibular range of motion and associated stretching and a self-modeling mouthguard to avoid cheek self-biting. This protocol allowed continuing the orthodontic treatment to restore the occlusion. Finally, good occlusion, normal function and better quality of patient's life were achieved.

摘要

先天性无痛症是一种罕见的临床综合征,其特征是自出生以来疼痛感知明显受损,通常由遗传性感觉和自主神经病引起,小纤维、伤害性神经纤维丧失。我们报告了一个 9 岁的病例,表现为全身性先天性无痛症。该患者因严重的张口受限和多发性口腔溃疡被私人正畸医生转诊至我科,在开始正畸治疗后,这些口腔溃疡严重恶化。描述了他的口腔病变的张口受限和正畸治疗的管理。治疗方法旨在改善下颌运动范围和相关的拉伸,并使用自我塑造的口腔保护器以避免颊部自我咬伤。该方案允许继续进行正畸治疗以恢复咬合。最终,实现了良好的咬合、正常的功能和患者生活质量的提高。

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