僵人谱系障碍:概述,重点是头颈部合并症

John K. Brooks DDS, Youstina Hanna, Amer Al-mefleh
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引用次数: 0

摘要

僵人谱系障碍(SPSD)是一种罕见的进行性自身免疫性神经肌肉综合征,主要表现为剧烈疼痛性痉挛以及轴性和附着性肌肉僵硬。受影响的个体易患一系列其他神经病变,包括小脑共济失调和癫痫活动、眼科异常和其他自身免疫性系统疾病,特别是 1 型糖尿病、甲状腺炎、恶性贫血和恶性肿瘤。口腔医学文献中有关 SPSD 的信息十分有限。因此,本文旨在综述SPSD的临床病理特征,尤其侧重于头颈部受累情况。此外,本文还提供了对患者进行牙科治疗的临床指南,并总结了头颈部的手术过程和结果。(Oral Surg Oral Med Oral Pathol Oral Radiol YEAR;VOL:page range)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stiff person spectrum disorder: overview with emphasis on head and neck comorbidities
Stiff person spectrum disorder (SPSD) is a rare progressive autoimmune neuromuscular syndrome, primarily resulting in severely painful spasms and rigidity of the axial and appendicular musculature. Affected individuals are predisposed to develop an array of other neuropathies, including cerebellar ataxia and seizure activity, ophthalmologic abnormalities, and other autoimmune-based systemic diseases, notably type 1 diabetes mellitus, thyroiditis, pernicious anemia, and malignancy. Limited information exists in the oral medicine literature regarding SPSD. Thus, the objective of this paper is to review the clinicopathologic features of SPSD, with particular emphasis on head and neck involvement. Additionally, clinical guidelines for dental management of affected individuals and a summary of surgical procedures and outcomes performed in the head and neck are provided. (Oral Surg Oral Med Oral Pathol Oral Radiol YEAR;VOL:page range)
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