증례

피열연골에 발생한 신경섬유종 1예

민한기1, 박병철1, 김남국1, 오현명1,*
Han Ki Min1, Byung Chul Park1, Nam Kook Kim1, Hyun Myung Oh1,*
Author Information & Copyright
1광주기독병원 이비인후과
1Department of Otorhinolaryngology, Kwangju Christian Hospital, Gwangju, Korea
*교신저자: 박병철, 503-715 광주광역시 남구 양림동 264 광주기독병원 이비인후과 전화 :(062) 650-5095·전송:(062) 650-5090 E-mail:kie0039@naver.com

© Copyright 2011 The Busan, Ulsan, Gyeoungnam Branch of Korean Society of Otolaryngology-Head and Neck Surgery. This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: Jun 02, 2011; Revised: Jul 22, 2011; Accepted: Aug 31, 2011

Published Online: May 31, 2020

ABSTRACT

Neurofibroma in the larynx is a rare disease. A case of solitary endolaryngeal neurofibroma was reported first by Suchanek in 1925. As the report, the commonly occured site is the aryepiglottic fold or the arytenoid cartilage, because the branch of the superior laryngeal nerve is involved. We present a case of incidently detected neurofibroma in arytenoid cartilage. The 68 year-old male with solitary neurofibroma in the arytenoid cartilage, had no laryngeal symptoms such as throat discomfort, globus sensation, and dyspnea. We present the case of solitary neurofibroma of the arytenoid cartilage. (J Clinical Otolaryngol 2011;22:268-270)

Keywords: 신경섬유종; 피열연골
Keywords: Neurofibroma; Arytenoid cartilage