Journal of Clinical Otolaryngology Head and Neck Surgery

The Busan, Ulsan, Gyeoungnam Branch of Korean Society of Otolaryngology-Head and Neck Surgery

J Clin Otolaryngol Head Neck Surg 2011; 22(2):196-200

pISSN: 1225-0244, eISSN: 2713-833X

DOI: https://doi.org/10.35420/jcohns.2011.22.2.196

원저

선천성진주종의 임상적 분석

고의경¹^,^*, 공수근¹, 박성환¹, 위찬은¹, 고진영¹, 이덕규¹, 이일우¹

Clinical Analysis of Congenital Cholesteatoma of the Middle Ear

Eui-Kyung Goh¹^,^*, Soo-Keun Kong¹, Sung-Hwan Park¹, Chan-Eun Wie¹, Jin-Young Goh¹, Duk-Gyu Lee¹, Il-Woo Lee¹

¹부산대학교 의학전문대학원 이비인후과학교실

¹Department of Otorhinolaryngology-Head and Neck Surgery, Pusan National University School of Medicine, Busan, Korea

^*교신저자: 고의경, 602-739 부산광역시 서구 아미동 1가 10 부산대학교 의학전문대학원 이 비 인후과학교실 전화: (051) 240-7536·전송: (051) 246-8668 E-mail： gohek@pusan.ac.kr

© 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: Aug 12, 2011; Revised: Sep 05, 2011; Accepted: Oct 10, 2011

Published Online: May 31, 2020

ABSTRACT

Backgrounds and Objectives: Recently congenital cholesteatoma of middle ear has been diagnosed in earlier stage and its clinical manifestation has showed changed clinical manifestation, comparing that of reported literature. Aim of this study were to elucidate of clinical finding, extent of the cholesteatoma, staging, operative procedure and rate of postoperative recurrence in congenital middle ear cholesteatoma. Materials and Methods: 47 cases of congenital cholesteatoma had been treated in Department of Otorhinolaryngolgy of Pusan National University Hospital from 1997 to October of 2010 and were reviewd retrospectively. Results : Congenital cholesteatoma showed male preponderance, and had diagnosed incidentaly (46.8%) and most common symptom was hearing loss. Most were found in tympanum only (70.2%) and more found in posterior portion than in anterior portion. Rate of each stage is similar distribution in stage I, II, III, IV. Recurrence rate showed 14.9%. Conclusions :Early diagnosis and early intervention is important to avoid recurrence and morbidity. (J Clinical Otolaryngol 2011;22:196–200)

Keywords: 진주종; 선천성; 중이; 재발

Keywords: Cholesteatoma; Congenital; Middle ear; Recurrence