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An extremely rare case of pulmonary epithelioid hemangioendothelioma
Epithelioid emangioendothelioma (EHE) is a rare tumor originating from vascular endothelial cells, which belongs to malignant vascular tumors with low to moderate differentiation and potential metastatic ability and its incidence rate is less than one in a million. We herein report a rare case of EH...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447165/ https://www.ncbi.nlm.nih.gov/pubmed/37488675 http://dx.doi.org/10.1111/1759-7714.15051 |
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author | Chen, Xi Wang, Yun Che, Guowei Shen, Cheng |
author_facet | Chen, Xi Wang, Yun Che, Guowei Shen, Cheng |
author_sort | Chen, Xi |
collection | PubMed |
description | Epithelioid emangioendothelioma (EHE) is a rare tumor originating from vascular endothelial cells, which belongs to malignant vascular tumors with low to moderate differentiation and potential metastatic ability and its incidence rate is less than one in a million. We herein report a rare case of EHE of pulmonary origin and a review of the literature concerning the clinical and pathological features of this disease. The patient underwent left upper lobectomy to completely extirpate the lesion by video‐assisted thoracic surgery. Our findings suggest the difficulty of making a diagnosis before surgery and that more cases need to be reported in order to facilitate the preoperative diagnosis of such a rare tumor. |
format | Online Article Text |
id | pubmed-10447165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-104471652023-08-24 An extremely rare case of pulmonary epithelioid hemangioendothelioma Chen, Xi Wang, Yun Che, Guowei Shen, Cheng Thorac Cancer Case Reports Epithelioid emangioendothelioma (EHE) is a rare tumor originating from vascular endothelial cells, which belongs to malignant vascular tumors with low to moderate differentiation and potential metastatic ability and its incidence rate is less than one in a million. We herein report a rare case of EHE of pulmonary origin and a review of the literature concerning the clinical and pathological features of this disease. The patient underwent left upper lobectomy to completely extirpate the lesion by video‐assisted thoracic surgery. Our findings suggest the difficulty of making a diagnosis before surgery and that more cases need to be reported in order to facilitate the preoperative diagnosis of such a rare tumor. John Wiley & Sons Australia, Ltd 2023-07-24 /pmc/articles/PMC10447165/ /pubmed/37488675 http://dx.doi.org/10.1111/1759-7714.15051 Text en © 2023 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Chen, Xi Wang, Yun Che, Guowei Shen, Cheng An extremely rare case of pulmonary epithelioid hemangioendothelioma |
title | An extremely rare case of pulmonary epithelioid hemangioendothelioma |
title_full | An extremely rare case of pulmonary epithelioid hemangioendothelioma |
title_fullStr | An extremely rare case of pulmonary epithelioid hemangioendothelioma |
title_full_unstemmed | An extremely rare case of pulmonary epithelioid hemangioendothelioma |
title_short | An extremely rare case of pulmonary epithelioid hemangioendothelioma |
title_sort | extremely rare case of pulmonary epithelioid hemangioendothelioma |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447165/ https://www.ncbi.nlm.nih.gov/pubmed/37488675 http://dx.doi.org/10.1111/1759-7714.15051 |
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