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Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site
Cardiac angiosarcoma is the most common among primary malignant cardiac tumors in adults. Malignant cardiac tumors commonly arise in the right-sided cardiac chambers unlike benign tumors that commonly arise in the left-sided chambers. Cardiac tumors on the left side need to be carefully assessed for...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307616/ https://www.ncbi.nlm.nih.gov/pubmed/32766106 http://dx.doi.org/10.4103/jcecho.jcecho_32_19 |
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author | Poonia, Amitabh Mishra, Rekha Giridhara, Priya Arora, Yogendra Kumar |
author_facet | Poonia, Amitabh Mishra, Rekha Giridhara, Priya Arora, Yogendra Kumar |
author_sort | Poonia, Amitabh |
collection | PubMed |
description | Cardiac angiosarcoma is the most common among primary malignant cardiac tumors in adults. Malignant cardiac tumors commonly arise in the right-sided cardiac chambers unlike benign tumors that commonly arise in the left-sided chambers. Cardiac tumors on the left side need to be carefully assessed for malignant features for deciding treatment strategy and prognostication. We present the case of a 62-year-old female with a large left atrial mass infiltrating the interatrial septum and adjacent myocardial wall. Histology was suggestive of angiosarcoma. Although a radical excision was done, the tumor recurred within 6 months of the postoperative period and she died shortly after the recurrence. |
format | Online Article Text |
id | pubmed-7307616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-73076162020-08-05 Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site Poonia, Amitabh Mishra, Rekha Giridhara, Priya Arora, Yogendra Kumar J Cardiovasc Echogr Case Report Cardiac angiosarcoma is the most common among primary malignant cardiac tumors in adults. Malignant cardiac tumors commonly arise in the right-sided cardiac chambers unlike benign tumors that commonly arise in the left-sided chambers. Cardiac tumors on the left side need to be carefully assessed for malignant features for deciding treatment strategy and prognostication. We present the case of a 62-year-old female with a large left atrial mass infiltrating the interatrial septum and adjacent myocardial wall. Histology was suggestive of angiosarcoma. Although a radical excision was done, the tumor recurred within 6 months of the postoperative period and she died shortly after the recurrence. Wolters Kluwer - Medknow 2020 2020-04-13 /pmc/articles/PMC7307616/ /pubmed/32766106 http://dx.doi.org/10.4103/jcecho.jcecho_32_19 Text en Copyright: © 2020 Journal of Cardiovascular Echography http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Poonia, Amitabh Mishra, Rekha Giridhara, Priya Arora, Yogendra Kumar Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site |
title | Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site |
title_full | Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site |
title_fullStr | Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site |
title_full_unstemmed | Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site |
title_short | Left Atrial Angiosarcoma: A Rare Cardiac Tumor at an Uncommon Site |
title_sort | left atrial angiosarcoma: a rare cardiac tumor at an uncommon site |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307616/ https://www.ncbi.nlm.nih.gov/pubmed/32766106 http://dx.doi.org/10.4103/jcecho.jcecho_32_19 |
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