Moses Caisha Nivenia, Mohamad Wan Syahmi Bin Wan, Baharuddin Kamarul Aryffin Bin, Mafauzy Mohamad Masykurin Bin, Shukri Mohd Faiz Bin Mohd
Department of Emergency Medicine, Universiti Sains Malaysia, Kota Bharu, Kelantan, Malaysia.
Turk J Emerg Med. 2025 Jul 1;25(3):239-241. doi: 10.4103/tjem.tjem_152_24. eCollection 2025 Jul-Sep.
A 32-year-old male presented with a 2-week history of progressive bilateral facial weakness, initially diagnosed as unilateral Bell's palsy. Upon development of bilateral symptoms, further investigations revealed normal hematological, biochemical, and imaging results, ruling out common infectious and autoimmune causes. Electromyography and nerve conduction studies were normal, and lumbar puncture results excluded Guillain-Barré syndrome. The patient was ultimately diagnosed with idiopathic bilateral facial nerve palsy (FNP) after exhaustive exclusion of other etiologies. Treatment with corticosteroids led to symptomatic improvement. This case underscores the importance of a systematic approach in diagnosing rare presentations of FNP and highlights the favorable prognosis with appropriate management.
一名32岁男性,有进行性双侧面部无力2周病史,最初被诊断为单侧贝尔麻痹。出现双侧症状后,进一步检查显示血液学、生化和影像学结果正常,排除了常见的感染和自身免疫性病因。肌电图和神经传导研究正常,腰椎穿刺结果排除了吉兰-巴雷综合征。在彻底排除其他病因后,该患者最终被诊断为特发性双侧面神经麻痹(FNP)。使用皮质类固醇治疗后症状有所改善。该病例强调了系统方法在诊断FNP罕见表现中的重要性,并突出了适当管理下的良好预后。