鼻上皮样血管内皮瘤1例报告及文献复习

Venkata Surabhi Rayal Akepati, Navaudhayam Ranganathan, Anu Agrawal, Raja Shekar C H T, Vikas Yadav
{"title":"鼻上皮样血管内皮瘤1例报告及文献复习","authors":"Venkata Surabhi Rayal Akepati,&nbsp;Navaudhayam Ranganathan,&nbsp;Anu Agrawal,&nbsp;Raja Shekar C H T,&nbsp;Vikas Yadav","doi":"10.1016/j.hmedic.2025.100212","DOIUrl":null,"url":null,"abstract":"<div><h3>Aim</h3><div>To understand the complexities in diagnosing and managing a rare case of Nasal epithelioid hemangioendothelioma, which can be clinically misdiagnosed as benign inflammatory conditions.</div></div><div><h3>Background</h3><div>Epithelioid hemangioendothelioma (EHE) is a rare locally invasive vascular tumor and it is characterized by proliferation of endothelial cells with epithelioid morphology. It is slow growing tumor with borderline malignant potential and has high chances of recurrence. Mostly seen in soft tissues of extremities, lungs and very rarely seen in head and neck. There are very few cases reported of EHE in nasal cavity.</div></div><div><h3>Case Description</h3><div>The present case report describes an unusual case of EHE of nasal cavity in a 37 year old male with 2 months history of nasal mass, obstruction and intermittent epistaxis. Patient underwent wide local excision of tumor and histopathology confirmed the diagnosis.</div></div><div><h3>Conclusion</h3><div>Usually wide local excision is the treatment of choice. Routinely regular follow up is advised. In cases of multiple recurrences and incompletely excised tumors radiation therapy is considered.</div></div><div><h3>Clinical Significance</h3><div>It is an indolent tumor which has potential for recurrence that is known to appear during adult life and unlikely to metastasize.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"12 ","pages":"Article 100212"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nasal epithelioid hemangioendothelioma - A rare case report and review of literature\",\"authors\":\"Venkata Surabhi Rayal Akepati,&nbsp;Navaudhayam Ranganathan,&nbsp;Anu Agrawal,&nbsp;Raja Shekar C H T,&nbsp;Vikas Yadav\",\"doi\":\"10.1016/j.hmedic.2025.100212\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aim</h3><div>To understand the complexities in diagnosing and managing a rare case of Nasal epithelioid hemangioendothelioma, which can be clinically misdiagnosed as benign inflammatory conditions.</div></div><div><h3>Background</h3><div>Epithelioid hemangioendothelioma (EHE) is a rare locally invasive vascular tumor and it is characterized by proliferation of endothelial cells with epithelioid morphology. It is slow growing tumor with borderline malignant potential and has high chances of recurrence. Mostly seen in soft tissues of extremities, lungs and very rarely seen in head and neck. There are very few cases reported of EHE in nasal cavity.</div></div><div><h3>Case Description</h3><div>The present case report describes an unusual case of EHE of nasal cavity in a 37 year old male with 2 months history of nasal mass, obstruction and intermittent epistaxis. Patient underwent wide local excision of tumor and histopathology confirmed the diagnosis.</div></div><div><h3>Conclusion</h3><div>Usually wide local excision is the treatment of choice. Routinely regular follow up is advised. In cases of multiple recurrences and incompletely excised tumors radiation therapy is considered.</div></div><div><h3>Clinical Significance</h3><div>It is an indolent tumor which has potential for recurrence that is known to appear during adult life and unlikely to metastasize.</div></div>\",\"PeriodicalId\":100908,\"journal\":{\"name\":\"Medical Reports\",\"volume\":\"12 \",\"pages\":\"Article 100212\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949918625000579\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949918625000579","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的了解罕见的鼻上皮样血管内皮瘤的诊断和治疗的复杂性,该病例在临床上可能被误诊为良性炎症。深上皮样血管内皮瘤是一种罕见的局部侵袭性血管肿瘤,其特征是内皮细胞增生,呈上皮样形态。它是一种生长缓慢的肿瘤,具有交界性恶性潜能,复发率高。多见于四肢、肺部软组织,很少见于头颈部。鼻腔内EHE的病例报道很少。病例描述本病例报告描述了一个不寻常的鼻腔EHE病例,37岁男性,有2个月的鼻肿块,梗阻和间歇性鼻出血史。患者行肿瘤局部大范围切除,组织病理学证实诊断。结论广泛性局部切除通常是治疗的首选。建议定期随访。在多次复发和未完全切除肿瘤的情况下,考虑放射治疗。临床意义这是一种惰性肿瘤,有复发的可能性,已知在成人生活中出现,不太可能转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nasal epithelioid hemangioendothelioma - A rare case report and review of literature

Aim

To understand the complexities in diagnosing and managing a rare case of Nasal epithelioid hemangioendothelioma, which can be clinically misdiagnosed as benign inflammatory conditions.

Background

Epithelioid hemangioendothelioma (EHE) is a rare locally invasive vascular tumor and it is characterized by proliferation of endothelial cells with epithelioid morphology. It is slow growing tumor with borderline malignant potential and has high chances of recurrence. Mostly seen in soft tissues of extremities, lungs and very rarely seen in head and neck. There are very few cases reported of EHE in nasal cavity.

Case Description

The present case report describes an unusual case of EHE of nasal cavity in a 37 year old male with 2 months history of nasal mass, obstruction and intermittent epistaxis. Patient underwent wide local excision of tumor and histopathology confirmed the diagnosis.

Conclusion

Usually wide local excision is the treatment of choice. Routinely regular follow up is advised. In cases of multiple recurrences and incompletely excised tumors radiation therapy is considered.

Clinical Significance

It is an indolent tumor which has potential for recurrence that is known to appear during adult life and unlikely to metastasize.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信