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비인강 혈관섬유종으로 오인된 혈관종성 상악동후비강폴립

김광훈1, 송영호1,*, 박기환1, 안회영1
Kwang Hoon Kim1, Young Ho Song1,*, Ki Hwan Park1, Hoe Young Ahn1
Author Information & Copyright
1경희대학교 의과대학 이비인후과학교실
1Department of Otolaryngology, College of Medicine, Kyunghee University, Seoul, Korea
*교신저자: 송영호, 130-702 서울 동대문구 회기동 1 경희대학교 의과대학 이비인후과학교실 전화: (02) 958-8474·전송: (02) 958-8470 E-mail: khuent@khmc.or.kr

© Copyright 2001 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: Feb 12, 2000; Accepted: May 12, 2001

Published Online: May 31, 2020

ABSTRACT

Antrochoanal polyp is rare disease and its angiomatous change is very rare condition. Most of the angiomatous antrochoanal polyps are developed in young age and related with frequent recurrent unilateral epistaxis and nasal obstruction. Having similar radiological findings to nasopharyngeal angiofibroma, angiomatous antrochoanal polyps are easy to be misconceived nasopharyngeal angiofibroma. The author recently experienced a case of angiomatous antrochoanal polyp which had similar findings to nasopharyngeal angiofibroma in CT scan and MRI scan but had few vasculature in angiography. Eventually it was removed completely by Caldwell-Luc operation and diagnosis was made as a angiomatous antrochoanal polyp through the pathologic results. (J Clinical Otolaryngol 2001;12:89-94)

Keywords: 혈관종성 상악동후비강폴립; 비인강 혈관 섬유종; 혈관조영술
Keywords: Angiomatous antrochoanal polyp; Nasopharyngeal angiofibroma; Angiography