종설

경부의 거대한 단발성 신경섬유종 1례

오경균1, 최진호1, 이장한1, 한영창2
Kyung Kyoon Oh1, Jin Ho Choi1, Jang Han Lee1, Young Chang Han2
Author Information & Copyright
1원자력병원 이비인후-두경부외과
2요셉이비인후과 의원
1Department of Otolaryngology-Head and Neck Surgery, Korea Cancer Center Hospital
2St. Joseph ENT Clinic

© Copyright 1998 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.

Published Online: May 31, 2020

ABSTRACT

A neurofibroma is a tumor of the nerve sheath. The neurofibroma originates from the Schwann cells, which produce the perineural connective tissue. Solitary neurofibromas that are limited to the head and neck area are rare. It is a well-defined, benign, slowly growing tumor, attached to the nerve of origin, which is generally asymptomatic.

A 23-year-old woman, with a 5-year history of neck masses, presented at the outpatient department. There were swallowing difficulty and intermittent dyspnea. On radiologic studies, huge mass occupying right side of the neck from the low-oropharynx to the superior mediastinum, extended into the contralateral side of the neck through the prevertebral space with displacement of the common carotid and vertebral artery and upper esophagus. Multiple surgical resection of the neck masses was performed through a low neck incision. Two relatively well circumscribed multinodular rubbery huge masses measuring 20x13x9 cm and 14x14x11 cm were revealed. Cut surface showed pinkish white dense collagenous tissue with yellowish myxoid areas. There was no evidence of recurrence for 9-year follow-ups.

Keywords: Solitary neurofibroma; Neurogenic tumor; Neck


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