Primitive Neuroectodermal Tumour of the Larynx: A Rare Case Report.

IF 0.6 Q4 ONCOLOGY Indian Journal of Surgical Oncology Pub Date : 2024-09-01 Epub Date: 2024-05-27 DOI:10.1007/s13193-024-01970-6
Swapnil Kaushal, Fernandes Ellerhea, Pol Jaydeep, Desai Abhineet
{"title":"Primitive Neuroectodermal Tumour of the Larynx: A Rare Case Report.","authors":"Swapnil Kaushal, Fernandes Ellerhea, Pol Jaydeep, Desai Abhineet","doi":"10.1007/s13193-024-01970-6","DOIUrl":null,"url":null,"abstract":"<p><p>Ewing's sarcoma/primitive neuroectodermal tumour is a malignant small round blue cell tumour of neuroectodermal origin that affects bones and soft tissue in children and young adults. These are aggressive malignant tumours, and long-term survival rates following diagnosis remain poor. Occurrence of primitive neuroectodermal tumours in the head and neck region is uncommon. It is extremely rare in the larynx with only 12 cases reported in the literature. We report a case of primary primitive neuroectodermal tumour of the larynx in a 28-year-old female. She presented with hoarseness of voice, and her computed tomography and laryngoscopy revealed a mass at the laryngeal inlet. A biopsy followed by histopathology and immunohistochemistry confirmed the diagnosis of a primitive neuroectodermal tumour. She initially defaulted from treatment and subsequently presented with stridor for which an emergency tracheostomy was done. Her metastatic workup did not reveal any lesion elsewhere. So, a diagnosis of a primary primitive neuroectodermal tumour of the larynx was made, and the patient was started on treatment.</p>","PeriodicalId":46707,"journal":{"name":"Indian Journal of Surgical Oncology","volume":"15 Suppl 3","pages":"385-389"},"PeriodicalIF":0.6000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11422299/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Surgical Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s13193-024-01970-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/5/27 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Ewing's sarcoma/primitive neuroectodermal tumour is a malignant small round blue cell tumour of neuroectodermal origin that affects bones and soft tissue in children and young adults. These are aggressive malignant tumours, and long-term survival rates following diagnosis remain poor. Occurrence of primitive neuroectodermal tumours in the head and neck region is uncommon. It is extremely rare in the larynx with only 12 cases reported in the literature. We report a case of primary primitive neuroectodermal tumour of the larynx in a 28-year-old female. She presented with hoarseness of voice, and her computed tomography and laryngoscopy revealed a mass at the laryngeal inlet. A biopsy followed by histopathology and immunohistochemistry confirmed the diagnosis of a primitive neuroectodermal tumour. She initially defaulted from treatment and subsequently presented with stridor for which an emergency tracheostomy was done. Her metastatic workup did not reveal any lesion elsewhere. So, a diagnosis of a primary primitive neuroectodermal tumour of the larynx was made, and the patient was started on treatment.

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
喉原始神经外胚层肿瘤:罕见病例报告
尤文氏肉瘤/原始神经外胚层瘤是一种起源于神经外胚层的恶性小圆形蓝细胞瘤,好发于儿童和青少年的骨骼和软组织。这类肿瘤是侵袭性恶性肿瘤,确诊后的长期存活率仍然很低。头颈部原始神经外胚层肿瘤并不常见。喉部的原始神经外胚层肿瘤极为罕见,文献中仅报道了12例。我们报告了一例 28 岁女性喉部原发性原始神经外胚层肿瘤。她出现声音嘶哑,计算机断层扫描和喉镜检查发现喉入口处有肿块。组织病理学和免疫组化检查证实了她的诊断:原始神经外胚层肿瘤。她起初没有接受治疗,后来出现了呼吸困难,为此进行了紧急气管切开术。她的转移性检查没有发现其他部位的病变。因此,她被诊断为喉部原发性原始神经外胚层肿瘤,并开始接受治疗。
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
1.10
自引率
0.00%
发文量
190
期刊介绍: The Indian Journal of Surgical Oncology aims to encourage and promote clinical and research activities pertaining to Surgical Oncology. It also aims to bring in the concept of multidisciplinary team approach in management of various cancers. The Journal would publish original article, point of technique, review article, case report, letter to editor, profiles of eminent teachers, surgeons and instititions - a short (up to 500 words) of the Cancer Institutions, departments, and oncologist, who founded new departments.
期刊最新文献
A Comprehensive Bioinformatic Analysis Identifies a Tumor Suppressor Landscape of the MEG3 lncRNA in Breast Cancer. A Short Course of Preoperative Denosumab Injection Followed by Surgery in High-Risk Giant Cell Tumors of the Extremities: A Retrospective Study. Adamantinoma: A SEER-based Epidemiological Analysis. Analyzing Androgen Receptor Expression in Breast Cancer: Insights into Histopathological Parameters and Hormone Receptor Status Among Indian Women. Association of Breast Cancer Subtypes and Clinicopathological Factors with Axillary Lymph Node Positivity Amongst Women with Breast Cancer in Rajasthan: An Observational Analytical Study.
×
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