Thyroid liposarcoma: a case report.

IF 1.7 Q2 SURGERY Innovative Surgical Sciences Pub Date : 2022-12-01 DOI:10.1515/iss-2021-0037
Maxime Gerard, Alexander N Flaris, Marco Demarchi, Ilies El Boukili, Laure Maillard, Françoise Borson-Chazot, Myriam Decaussin-Petrucci, Jean-Christophe Lifante
{"title":"Thyroid liposarcoma: a case report.","authors":"Maxime Gerard,&nbsp;Alexander N Flaris,&nbsp;Marco Demarchi,&nbsp;Ilies El Boukili,&nbsp;Laure Maillard,&nbsp;Françoise Borson-Chazot,&nbsp;Myriam Decaussin-Petrucci,&nbsp;Jean-Christophe Lifante","doi":"10.1515/iss-2021-0037","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Thyroid liposarcoma is a rare tumor. Its low prevalence accounts for the scarcity of data in the literature, which consists mostly of small studies and case reports.</p><p><strong>Case presentation: </strong>We present the case of a 60 years old male with no past medical or past surgical history and presented with neck discomfort and a large left thyroid nodule. Thyroid ultrasound and CT scan were performed and confirmed the existence of a thyroid nodule most probably inside the left inferior thyroid lobe. In the posterior mediastinum, two fatty formations were found. To complete, an MRI was performed, showing a mixed lesion, of the lower neck and upper chest. The patient underwent an extended resection which consisted of an en bloc resection of the lesion (left thyroid lobectomy and isthmus resection) by an anterior transverse cervical incision and a sternotomy. Tracheal and laryngeal shaving and esophageal shaving with resection of the esophageal muscularis was performed as well. The pathological evaluation of the specimen showed a grade II dedifferentiated liposarcoma with an inflammatory component.</p><p><strong>Conclusions: </strong>Thyroid liposarcoma is a rare lesion of the thyroid. Its management requires an exhaustive workup followed by an en bloc resection of the lesion. Depending on the histology, postoperative radiation therapy may or may not be necessary.</p>","PeriodicalId":44186,"journal":{"name":"Innovative Surgical Sciences","volume":"7 3-4","pages":"133-137"},"PeriodicalIF":1.7000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742268/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Innovative Surgical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/iss-2021-0037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Thyroid liposarcoma is a rare tumor. Its low prevalence accounts for the scarcity of data in the literature, which consists mostly of small studies and case reports.

Case presentation: We present the case of a 60 years old male with no past medical or past surgical history and presented with neck discomfort and a large left thyroid nodule. Thyroid ultrasound and CT scan were performed and confirmed the existence of a thyroid nodule most probably inside the left inferior thyroid lobe. In the posterior mediastinum, two fatty formations were found. To complete, an MRI was performed, showing a mixed lesion, of the lower neck and upper chest. The patient underwent an extended resection which consisted of an en bloc resection of the lesion (left thyroid lobectomy and isthmus resection) by an anterior transverse cervical incision and a sternotomy. Tracheal and laryngeal shaving and esophageal shaving with resection of the esophageal muscularis was performed as well. The pathological evaluation of the specimen showed a grade II dedifferentiated liposarcoma with an inflammatory component.

Conclusions: Thyroid liposarcoma is a rare lesion of the thyroid. Its management requires an exhaustive workup followed by an en bloc resection of the lesion. Depending on the histology, postoperative radiation therapy may or may not be necessary.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
甲状腺脂肪肉瘤1例。
目的:甲状腺脂肪肉瘤是一种罕见的肿瘤。它的低流行率解释了文献中数据的缺乏,这些文献主要由小型研究和病例报告组成。病例介绍:我们报告一名60岁男性,无既往病史或既往手术史,颈部不适,左侧甲状腺大结节。行甲状腺超声及CT扫描,证实有甲状腺结节,极可能位于左甲状腺下叶内。后纵隔可见两处脂肪形成。最后,进行了MRI检查,显示下颈部和上胸部的混合性病变。患者接受了扩大切除术,包括通过颈椎前横切口和胸骨切开术对病变进行整体切除(左甲状腺叶切除术和峡部切除术)。同时行气管、喉部刮除及食管刮除并切除食管肌层。病理检查显示为II级去分化脂肪肉瘤伴炎性成分。结论:甲状腺脂肪肉瘤是一种罕见的甲状腺病变。其管理需要彻底的检查,然后对病变进行整体切除。根据组织学,术后放射治疗可能是必要的,也可能不是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
5.40
自引率
0.00%
发文量
29
审稿时长
11 weeks
期刊最新文献
Periprosthetic joint infections - a scoping review. What's new in surgery? Essentials 2024 - young patients and fast decisions. A narrative review of present knowledge and digital approaches in orthognathic surgery. Update burn surgery: overview of current multidisciplinary treatment concepts. Early enteral nutrition (EEN) following intestinal anastomosis in pediatric patients - what's new?
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1