Case Report
Copyright ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Sep 6, 2019; 7(17): 2652-2657
Published online Sep 6, 2019. doi: 10.12998/wjcc.v7.i17.2652
An extremely rare pedunculated lipoma of the hypopharynx: A case report
Qiang Sun, Chun-Lin Zhang, Zhao-Hui Liu
Qiang Sun, Chun-Lin Zhang, Zhao-Hui Liu, Department of Otolaryngology Head and Neck Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China
Author contributions: Liu ZH designed the study; Liu ZH, Liang YZ, and Sun Q contributed surgical treatment and follow-up data collection; Sun Q wrote the paper; Zhang CL revised the manuscript; all authors read and approved the final manuscript.
Informed consent statement: The patient gave informed consent. Consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: The authors have no conflicts of interest to declare. None of the authors have received funding from any organization with a real or potential interest in the subject matter, materials, equipment, software, or devices discussed.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Corresponding author: Zhao-Hui Liu, MSc, Chairman, Chief Doctor, Doctor, Full Professor, Senior Lecturer, Department of Otolaryngology Head and Neck Surgery, Affiliated Hospital of Zunyi Medical University, 149 Dalian Road, Huichuan District, Zunyi 563000, Guizhou Province, China. rzent@163.com
Telephone: +86-851-28608114
Received: April 22, 2019
Peer-review started: April 23, 2019
First decision: June 12, 2019
Revised: June 16, 2019
Accepted: June 26, 2019
Article in press: June 26, 2019
Published online: September 6, 2019
Abstract
BACKGROUND

Hypopharyngeal lipoma is a rare disease that can lead to asphyxiation after aspiration. Sclerotic lipoma in the hypopharynx is an extremely rare histological type. Hypopharyngeal lipoma should be resected in time after diagnosis.

CASE SUMMARY

An 86-year-old female patient presented to our department with a long pedunculated mass protruding from her mouth. Until this time, the patient had no dyspnea, dysphagia, or throat discomfort. Physical examination showed stable vital signs and clear consciousness. The pedicel was derived from the posterior wall of the hypopharynx. The tumor was smooth, hyperemic and dark red, about 10 cm long, and 4 cm wide. In order to prevent airway obstruction, the hypopharyngeal tumor was excised in emergent operation. The pharyngeal cavity was exposed by a mouth gag during the operation. A disposable plasma knife was used to completely remove the tumor along the base of the new organism, and no active bleeding occurred. The postoperative pathological results were sclerotic lipoma.

CONCLUSION

Lipoma in the pharynx is relatively rare. Patients with this condition must be referred immediately to Ear-Nose-Throat specialists and complete surgical excision should be performed as soon as possible to prevent serious complications, such as airway obstruction and death.

Keywords: Hypopharynx tumor, Sclerotic lipoma, Plasma, Case report

Core tip: Sclerotic lipoma in the hypopharynx is extremely rare. We report a case of hypopharyngeal sclerotic lipoma in a female patient. The lipoma was removed with plasma radiofrequency at low temperature under general anesthesia. The patient had no discomfort in the hypopharynx after surgery. The pathologic findings, clinical feature, and treatment of the disease are presented and discussed.