Long Ling, Kang Zhuang, Chen Shaoqiong, Cui Chunping, Men Xuejiao, Qiu Wei
Department of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Radiology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Front Neurol. 2020 Aug 4;11:797. doi: 10.3389/fneur.2020.00797. eCollection 2020.
Parry-Romberg syndrome (PRS) is a rare disease that causes hemiatrophy of the face. The pathophysiological mechanisms involved in its etiology are unknown, but several previous reports suggest the involvement of autoimmune factors. Herein we describe the case of a patient with PRS who was initially misdiagnosed as having multiple sclerosis (MS). The relevant literature is briefly reviewed, and some previous reports suggesting associations between PRS and autoimmunity are discussed. A 34-year-old man presented with recurrent paroxysmal weakness of the right hand, a 3-years history of unilateral tinnitus, and headache for 6 months. MS was initially diagnosed but the patient was subsequently diagnosed as having PRS on the basis of clinical manifestations and radiological findings. PRS may be associated with autoimmune pathogenesis, but the present case does not support that theory.
帕里-龙贝格综合征(PRS)是一种导致面部半侧萎缩的罕见疾病。其病因涉及的病理生理机制尚不清楚,但先前的一些报告提示自身免疫因素的参与。在此,我们描述了一例最初被误诊为多发性硬化症(MS)的PRS患者。简要回顾了相关文献,并讨论了先前一些提示PRS与自身免疫之间存在关联的报告。一名34岁男性,出现右手反复阵发性无力、3年单侧耳鸣病史以及6个月头痛症状。最初诊断为MS,但随后根据临床表现和影像学检查结果诊断为PRS。PRS可能与自身免疫发病机制有关,但本病例并不支持该理论。