Epithelioid hemangioendothelioma of the sternum
Abstract Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor composed of dendritic and endothelial cells, and accounts for less than 1% of all vascular tumors. The tumor may arise from any location in the body, but it has a predilection for veins of the extremities, the liver, bone, and...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-06-01
|
Series: | Thoracic Cancer |
Subjects: | |
Online Access: | https://doi.org/10.1111/1759-7714.13454 |
id |
doaj-3c87aab11cca4775abea2b239b6c2849 |
---|---|
record_format |
Article |
spelling |
doaj-3c87aab11cca4775abea2b239b6c28492020-11-25T03:29:44ZengWileyThoracic Cancer1759-77061759-77142020-06-011161741174510.1111/1759-7714.13454Epithelioid hemangioendothelioma of the sternumWenpeng Song0Zeng Zhen1Lin Li2Jing Ye3Sicheng Zhou4Qiyou Wu5Liu Xu6Huilin Li7Feng Lin8Department of Thoracic Surgery West China Hospital, Sichuan University Chengdu ChinaDepartment of Thoracic Surgery West China Hospital, Sichuan University Chengdu ChinaPathology Department West China Hospital, Sichuan University Chengdu ChinaWest China School of Medicine Sichuan University Chengdu ChinaWest China School of Medicine Sichuan University Chengdu ChinaWest China School of Medicine Sichuan University Chengdu ChinaWest China School of Medicine Sichuan University Chengdu ChinaWest China School of Medicine Sichuan University Chengdu ChinaDepartment of Thoracic Surgery West China Hospital, Sichuan University Chengdu ChinaAbstract Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor composed of dendritic and endothelial cells, and accounts for less than 1% of all vascular tumors. The tumor may arise from any location in the body, but it has a predilection for veins of the extremities, the liver, bone, and skin. Herein, we report a case of a 43‐year‐old man who presented with a chest mass accompanied by chest pain. Computed tomography (CT) scan of the chest showed a 3 cm × 2 cm sternal mass in the chest wall. We performed tumor resection and reconstruction of the chest wall. EHE was confirmed via postoperative pathology. The patient underwent postoperative adjuvant radiotherapy, and no evidence of tumor recurrence was discovered during the one‐year follow up.https://doi.org/10.1111/1759-7714.13454Epithelioid hemangioendotheliomafollow‐upsternumsurgical resection |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wenpeng Song Zeng Zhen Lin Li Jing Ye Sicheng Zhou Qiyou Wu Liu Xu Huilin Li Feng Lin |
spellingShingle |
Wenpeng Song Zeng Zhen Lin Li Jing Ye Sicheng Zhou Qiyou Wu Liu Xu Huilin Li Feng Lin Epithelioid hemangioendothelioma of the sternum Thoracic Cancer Epithelioid hemangioendothelioma follow‐up sternum surgical resection |
author_facet |
Wenpeng Song Zeng Zhen Lin Li Jing Ye Sicheng Zhou Qiyou Wu Liu Xu Huilin Li Feng Lin |
author_sort |
Wenpeng Song |
title |
Epithelioid hemangioendothelioma of the sternum |
title_short |
Epithelioid hemangioendothelioma of the sternum |
title_full |
Epithelioid hemangioendothelioma of the sternum |
title_fullStr |
Epithelioid hemangioendothelioma of the sternum |
title_full_unstemmed |
Epithelioid hemangioendothelioma of the sternum |
title_sort |
epithelioid hemangioendothelioma of the sternum |
publisher |
Wiley |
series |
Thoracic Cancer |
issn |
1759-7706 1759-7714 |
publishDate |
2020-06-01 |
description |
Abstract Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor composed of dendritic and endothelial cells, and accounts for less than 1% of all vascular tumors. The tumor may arise from any location in the body, but it has a predilection for veins of the extremities, the liver, bone, and skin. Herein, we report a case of a 43‐year‐old man who presented with a chest mass accompanied by chest pain. Computed tomography (CT) scan of the chest showed a 3 cm × 2 cm sternal mass in the chest wall. We performed tumor resection and reconstruction of the chest wall. EHE was confirmed via postoperative pathology. The patient underwent postoperative adjuvant radiotherapy, and no evidence of tumor recurrence was discovered during the one‐year follow up. |
topic |
Epithelioid hemangioendothelioma follow‐up sternum surgical resection |
url |
https://doi.org/10.1111/1759-7714.13454 |
work_keys_str_mv |
AT wenpengsong epithelioidhemangioendotheliomaofthesternum AT zengzhen epithelioidhemangioendotheliomaofthesternum AT linli epithelioidhemangioendotheliomaofthesternum AT jingye epithelioidhemangioendotheliomaofthesternum AT sichengzhou epithelioidhemangioendotheliomaofthesternum AT qiyouwu epithelioidhemangioendotheliomaofthesternum AT liuxu epithelioidhemangioendotheliomaofthesternum AT huilinli epithelioidhemangioendotheliomaofthesternum AT fenglin epithelioidhemangioendotheliomaofthesternum |
_version_ |
1724577367308894208 |