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Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report
Epithelioid hemangioendothelioma (EHE) is a rare malignant cancer of vascular origin that can affect multiple and varied tissue sites. A subtype of EHE, pulmonary epithelioid hemangioendothelioma (PHE), is more unusual with only 200 reported cases. Of these, only 27 have been classified as pleural i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432902/ https://www.ncbi.nlm.nih.gov/pubmed/26015825 http://dx.doi.org/10.14740/jocmr2174w |
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author | Salijevska, Julita Watson, Robert Clifford, Amy Ritchie, Andrew I. Mauri, Francisco Adeboyeku, David |
author_facet | Salijevska, Julita Watson, Robert Clifford, Amy Ritchie, Andrew I. Mauri, Francisco Adeboyeku, David |
author_sort | Salijevska, Julita |
collection | PubMed |
description | Epithelioid hemangioendothelioma (EHE) is a rare malignant cancer of vascular origin that can affect multiple and varied tissue sites. A subtype of EHE, pulmonary epithelioid hemangioendothelioma (PHE), is more unusual with only 200 reported cases. Of these, only 27 have been classified as pleural in origin. Based on available literature, the average age of presentation of pleural PHE is 45.7 years with a male preponderance of 2.375. A summary of all published case reports reveals significant heterogeneity both in presentation and management. Here we add to this knowledge-base with a report of an unusual case of pleural PHE in a 36-year-old female who presented with a 6-week history of chest pain and breathlessness. Significant challenges in the diagnosis and management of patients with pleural PHE exist, including a wide initial differential diagnosis and difficulties in obtaining tissue specimens, coupled with relatively limited treatment options. Early referral to a cardiothoracic center for video-assisted thoracoscopic biopsy is crucial in facilitating a diagnosis and allowing adequate pleural drainage for symptomatic relief. |
format | Online Article Text |
id | pubmed-4432902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44329022015-05-26 Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report Salijevska, Julita Watson, Robert Clifford, Amy Ritchie, Andrew I. Mauri, Francisco Adeboyeku, David J Clin Med Res Case Report Epithelioid hemangioendothelioma (EHE) is a rare malignant cancer of vascular origin that can affect multiple and varied tissue sites. A subtype of EHE, pulmonary epithelioid hemangioendothelioma (PHE), is more unusual with only 200 reported cases. Of these, only 27 have been classified as pleural in origin. Based on available literature, the average age of presentation of pleural PHE is 45.7 years with a male preponderance of 2.375. A summary of all published case reports reveals significant heterogeneity both in presentation and management. Here we add to this knowledge-base with a report of an unusual case of pleural PHE in a 36-year-old female who presented with a 6-week history of chest pain and breathlessness. Significant challenges in the diagnosis and management of patients with pleural PHE exist, including a wide initial differential diagnosis and difficulties in obtaining tissue specimens, coupled with relatively limited treatment options. Early referral to a cardiothoracic center for video-assisted thoracoscopic biopsy is crucial in facilitating a diagnosis and allowing adequate pleural drainage for symptomatic relief. Elmer Press 2015-07 2015-05-08 /pmc/articles/PMC4432902/ /pubmed/26015825 http://dx.doi.org/10.14740/jocmr2174w Text en Copyright 2015, Salijevska et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Salijevska, Julita Watson, Robert Clifford, Amy Ritchie, Andrew I. Mauri, Francisco Adeboyeku, David Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report |
title | Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report |
title_full | Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report |
title_fullStr | Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report |
title_full_unstemmed | Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report |
title_short | Pleural Epithelioid Hemangioendothelioma: Literature Summary and Novel Case Report |
title_sort | pleural epithelioid hemangioendothelioma: literature summary and novel case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432902/ https://www.ncbi.nlm.nih.gov/pubmed/26015825 http://dx.doi.org/10.14740/jocmr2174w |
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