台耳醫誌

雜誌專區 -第59卷第4期

病例報告 
Nasal Schwannoma―Case Report and Literature Review  僅供有效會員 登入會員查看全文
196~200 
英文 
Schwannoma、Nasal、Neurilemmoma 
Cheng-Chieh Huang1 、Yueh-Lee2 、Chia-Chen Hsu1,3 、Hung-Meng Huang1,4 、Tzong-Hann Yang1,3,5,6  
Department of Otorhinolaryngology, Taipei City Hospital1 、Department of Anatomical Pathology, Taipei City Hospital2 、Department of Exercise and Health Sciences, University of Taipei3 、Department of Otorhinolaryngology, Taipei Medical University, School of Medicine4 、Department of Speech, Language Pathology and Audiology, National Taipei University of Nursing and Health Science5 、Department of Otorhinolaryngology, National Yang Ming Chiao Tung University, School of Medicine, TAIWAN6  
Schwannoma is a benign, slow-growing tumor originating from nerve-supporting cell. Approximately 25-40% of schwannomas develop in the head and neck region. However, only about 4% occur in the sinonasal tract. This study presents a rare case of nasal schwannoma along with a review of the relevant literature. We discuss a 54-year-old woman with no underlying diseases who presented with left-sided nasal obstruction and recurrent epistaxis for 2 months without nasal discharge, hyposmia/anosmia, or headache. Sinus computed tomography imaging showed a mass in the nasal cavity attached to the left inferior turbinate and nasal endoscopy revealed a protruding mass in left nasal cavity. Endoscopic-assisted wide excision and partial turbinectomy were performed under local anesthesia, with no recurrence noted 6 months postoperatively. Endoscopic-assisted surgery is a viable option for selected patients due to cosmetic considerations. Given its rarity and the difficulty of diagnosis based solely on physical examination and imaging, we present this case and describe the most relevant epidemiological and clinical characteristics of nasal schwannoma. (JTaiwan Otolaryngol Head Neck Surg 2025; 59:196-200)