증례

소아에서 발생한 Inflammatory Myofibroblastic Tumor in the Larynx

김재욱1, 김민식1, 이유미1, 이진춘1,*
Jae-Wook Kim1, Minsic Kim1, Yumi Lee1, Jin-Choon Lee1,*
Author Information & Copyright
1부산대학교 의학전문대학원 이비인후과학교실
1Department of Otorhinolaryngology-Head and Neck Surgery, Pusan National University School of Medicine, Busan, Korea
*교신저자: 이진춘, 50612 경남 양산시 물급읍 금오로 20 부산대학교 의학전문대학원 양산부산대학교병원 이비인후과학교실 전화 :(055) 360-2652·전송 :(055) 360-2126 E-mail:ljc0209@hanmail.net

© Copyright 2017 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: Sep 20, 2017; Revised: Oct 18, 2017; Accepted: Nov 10, 2017

Published Online: May 31, 2020

ABSTRACT

Inflammatory myofiber tumor (IMT) is a rare borderline tumor with uncertain behavior. This tumor is also known as inflammatory tumor, hematocyte granuloma, and sometimes referred to as inflammatory fibrosarcoma. IMT is a rare tumor of mesenchymal origin and is most commonly found in the lungs of children and adolescents. It is known that it may occur mainly in the mesentery and retina, but not in the head and neck region. Herein, we report a rare case of inflammatory myofibroblastic cells in the larynx in a 9 year-old child. (J Clinical Otolaryngol 2017;28:302-306)

Keywords: 후두; 소아; 염증성 근섬유모세표 종양
Keywords: Larynx; Child; Inflammatory myofibroblastic tumor