The Pleural Origin of Retiform Hemangioendothelioma: An Unusual Origin of a Rare Diagnosis.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-07-12 eCollection Date: 2024-01-01 DOI:10.1159/000539771
Hidayat Ullah, Imran Khan, Aria Khan, Apoorva Tangri, Saral Lamichhane, Shahzaib Maqbool, Abdulqadir J Nashwan
{"title":"The Pleural Origin of Retiform Hemangioendothelioma: An Unusual Origin of a Rare Diagnosis.","authors":"Hidayat Ullah, Imran Khan, Aria Khan, Apoorva Tangri, Saral Lamichhane, Shahzaib Maqbool, Abdulqadir J Nashwan","doi":"10.1159/000539771","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Vascular malignancies are categorized into benign hemangiomas, malignant angiosarcomas, and tumors of intermediate malignancy. Retiform hemangioendothelioma (RH) is one of the rare diagnoses belonging to the class of intermediate malignancies that was initially diagnosed.</p><p><strong>Case presentation: </strong>In this case report, we have reported a rare case of RH, a locally aggressive, vascular tumor of malignant potential presenting at an unusual site. The most observed locations of this soft tissue tumor are skin and subcutaneous tissues of extremities; however, this case of RH was observed in an unusual site called pleura, which is a rare occurrence related to this tumor. The presence of cell surface markers like CD31 and ERG of vascular and endothelial origin and the presence of hobnail appearance of endothelial channels on the biopsy profile supported the vascular origin of the tumor; the clinical features and imaging studies further confirmed the diagnosis of RH.</p><p><strong>Conclusion: </strong>In this case report, a rare case of RH with an unusual site of origin was highlighted. RH is a vascular neoplasm; commonly observed sites of this vascular tumor were skin and subcutaneous tissue of the extremities; however, in this case, the site was unusually different, which was the pleura of the left lung.</p>","PeriodicalId":9625,"journal":{"name":"Case Reports in Oncology","volume":null,"pages":null},"PeriodicalIF":0.7000,"publicationDate":"2024-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11249460/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000539771","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Vascular malignancies are categorized into benign hemangiomas, malignant angiosarcomas, and tumors of intermediate malignancy. Retiform hemangioendothelioma (RH) is one of the rare diagnoses belonging to the class of intermediate malignancies that was initially diagnosed.

Case presentation: In this case report, we have reported a rare case of RH, a locally aggressive, vascular tumor of malignant potential presenting at an unusual site. The most observed locations of this soft tissue tumor are skin and subcutaneous tissues of extremities; however, this case of RH was observed in an unusual site called pleura, which is a rare occurrence related to this tumor. The presence of cell surface markers like CD31 and ERG of vascular and endothelial origin and the presence of hobnail appearance of endothelial channels on the biopsy profile supported the vascular origin of the tumor; the clinical features and imaging studies further confirmed the diagnosis of RH.

Conclusion: In this case report, a rare case of RH with an unusual site of origin was highlighted. RH is a vascular neoplasm; commonly observed sites of this vascular tumor were skin and subcutaneous tissue of the extremities; however, in this case, the site was unusually different, which was the pleura of the left lung.

网状血管内皮瘤的胸膜起源:罕见诊断的不寻常起源
导言:血管恶性肿瘤分为良性血管瘤、恶性血管肉瘤和中间恶性肿瘤。视网膜状血管内皮瘤(RH)是属于中间恶性肿瘤的罕见诊断之一,最初被诊断为中间恶性肿瘤:在本病例报告中,我们报告了一例罕见的视网膜状血管内皮瘤(RH),这是一种局部侵袭性血管肿瘤,具有恶性潜能,发病部位不寻常。这种软组织肿瘤最常见的部位是四肢的皮肤和皮下组织;然而,本病例中的 RH 却出现在一个不寻常的部位--胸膜,这与这种肿瘤有关,实属罕见。活组织切片上出现的血管和内皮来源的细胞表面标志物(如 CD31 和 ERG)以及内皮通道的滚刀样外观支持了肿瘤的血管来源;临床特征和影像学检查进一步证实了 RH 的诊断:本病例报告重点介绍了一例罕见的 RH,其起源部位并不寻常。RH是一种血管性肿瘤;这种血管性肿瘤的常见部位是四肢的皮肤和皮下组织;然而,本病例的发病部位却与众不同,是左肺的胸膜。
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 求助全文
来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
×
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