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An exceptionally giant left atrial myxoma: a case report and literature review
BACKGROUND: Cardiac myxomas are considered the most common benign heart tumours. The clinical manifestations mainly depend on the size of the tumour. They usually vary from asymptomatic, mild non-specific symptoms, to severe obstructive cardiac and systemic findings. We describe herein a significant...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891267/ https://www.ncbi.nlm.nih.gov/pubmed/33629011 http://dx.doi.org/10.1093/ehjcr/ytaa401 |
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author | Al-Zamkan, Bassil Khalil Hashem, Anas Mohamad Alaaeldin, Samir Ahmed Abdel Aziz, Mohamed |
author_facet | Al-Zamkan, Bassil Khalil Hashem, Anas Mohamad Alaaeldin, Samir Ahmed Abdel Aziz, Mohamed |
author_sort | Al-Zamkan, Bassil Khalil |
collection | PubMed |
description | BACKGROUND: Cardiac myxomas are considered the most common benign heart tumours. The clinical manifestations mainly depend on the size of the tumour. They usually vary from asymptomatic, mild non-specific symptoms, to severe obstructive cardiac and systemic findings. We describe herein a significantly large left atrial myxoma in a patient misdiagnosed with respiratory asthma. CASE SUMMARY: A 54-year-old lady, was diagnosed previously with asthma, presented with a history of dyspnoea on exertion, palpitations, and mild peripheral oedema. Chest X-ray suggested pulmonary congestion. Due to high suspicion of cardiac issues, transthoracic echocardiography was done revealing giant left atrial mass. Consequently, the mass was approached and excised surgically through the inverted T biatrial incision. Grossly, the mass measured 10 × 8 × 6 cm, and it had a smooth surface and was filled with gelatinous material. The histopathology confirmed benign myxoma without malignant features. DISCUSSION: Our article mainly focuses on the diagnostic challenges of a patient with atrial myxoma. The major discrepancy between the tumour size and the severity of the patient’s symptoms should draw physicians’ attention to consider atrial myxoma over a long list of differentials, in order to take immediate action to reduce the mortality and improve the overall prognosis. |
format | Online Article Text |
id | pubmed-7891267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78912672021-02-23 An exceptionally giant left atrial myxoma: a case report and literature review Al-Zamkan, Bassil Khalil Hashem, Anas Mohamad Alaaeldin, Samir Ahmed Abdel Aziz, Mohamed Eur Heart J Case Rep Case Reports BACKGROUND: Cardiac myxomas are considered the most common benign heart tumours. The clinical manifestations mainly depend on the size of the tumour. They usually vary from asymptomatic, mild non-specific symptoms, to severe obstructive cardiac and systemic findings. We describe herein a significantly large left atrial myxoma in a patient misdiagnosed with respiratory asthma. CASE SUMMARY: A 54-year-old lady, was diagnosed previously with asthma, presented with a history of dyspnoea on exertion, palpitations, and mild peripheral oedema. Chest X-ray suggested pulmonary congestion. Due to high suspicion of cardiac issues, transthoracic echocardiography was done revealing giant left atrial mass. Consequently, the mass was approached and excised surgically through the inverted T biatrial incision. Grossly, the mass measured 10 × 8 × 6 cm, and it had a smooth surface and was filled with gelatinous material. The histopathology confirmed benign myxoma without malignant features. DISCUSSION: Our article mainly focuses on the diagnostic challenges of a patient with atrial myxoma. The major discrepancy between the tumour size and the severity of the patient’s symptoms should draw physicians’ attention to consider atrial myxoma over a long list of differentials, in order to take immediate action to reduce the mortality and improve the overall prognosis. Oxford University Press 2020-12-13 /pmc/articles/PMC7891267/ /pubmed/33629011 http://dx.doi.org/10.1093/ehjcr/ytaa401 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Reports Al-Zamkan, Bassil Khalil Hashem, Anas Mohamad Alaaeldin, Samir Ahmed Abdel Aziz, Mohamed An exceptionally giant left atrial myxoma: a case report and literature review |
title | An exceptionally giant left atrial myxoma: a case report and literature review |
title_full | An exceptionally giant left atrial myxoma: a case report and literature review |
title_fullStr | An exceptionally giant left atrial myxoma: a case report and literature review |
title_full_unstemmed | An exceptionally giant left atrial myxoma: a case report and literature review |
title_short | An exceptionally giant left atrial myxoma: a case report and literature review |
title_sort | exceptionally giant left atrial myxoma: a case report and literature review |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891267/ https://www.ncbi.nlm.nih.gov/pubmed/33629011 http://dx.doi.org/10.1093/ehjcr/ytaa401 |
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