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Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports
BACKGROUND: Cardiac myxoma is the most common type of primary cardiac tumor, with the majority located in the atrial wall. The tumor is attached to valvular structures in a few cases, of which the pulmonary valve is the least affected. Pulmonary valve myxoma may have different clinical manifestation...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026419/ https://www.ncbi.nlm.nih.gov/pubmed/36941612 http://dx.doi.org/10.1186/s12957-023-02984-0 |
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author | Saputra, Pandit Bagus Tri Jannah, Ayik Rochyatul Rofananda, Ihsan Fahmi Al-Farabi, Makhyan Jibril Wungu, Citrawati Dyah Kencono Susilo, Hendri Alsagaff, Mochamad Yusuf Gusnanto, Arief Oktaviono, Yudi Her |
author_facet | Saputra, Pandit Bagus Tri Jannah, Ayik Rochyatul Rofananda, Ihsan Fahmi Al-Farabi, Makhyan Jibril Wungu, Citrawati Dyah Kencono Susilo, Hendri Alsagaff, Mochamad Yusuf Gusnanto, Arief Oktaviono, Yudi Her |
author_sort | Saputra, Pandit Bagus Tri |
collection | PubMed |
description | BACKGROUND: Cardiac myxoma is the most common type of primary cardiac tumor, with the majority located in the atrial wall. The tumor is attached to valvular structures in a few cases, of which the pulmonary valve is the least affected. Pulmonary valve myxoma may have different clinical manifestations from the more common cardiac myxomas because of its vital position. A misdiagnosis of these types of cardiac myxoma may be detrimental to the care and well-being of patients. Therefore, this systematic review aims to define the clinical characteristics of pulmonary valve myxoma and how this differs from a more common cardiac myxoma. METHODS: Employed literature was obtained from PubMed, ScienceDirect, Scopus, Springer, and ProQuest without a publication year limit on August 23, 2022. The keyword was “pulmonary valve myxoma.” Inclusion criteria were as follows: (1) case report or series, (2) available individual patient data, and (3) myxoma that is attached to pulmonary valve structures with no evidence of metastasis. Non-English language or nonhuman subject studies were excluded. Johanna Briggs Institute checklists were used for the risk of bias assessment. Data are presented descriptively. RESULTS: This review included 9 case reports from 2237 articles. All cases show a low risk of bias. Pulmonary valve myxoma is dominated by males (5:4), and the patient’s median age is 57 years with a bimodal distribution in pediatric and geriatric populations. The clinical manifestation of pulmonary valve myxoma is often unspecified or asymptomatic. However, systolic murmur in the pulmonary valve area is heard in 67% of cases. Echocardiography remains the diagnostic modality of choice in the majority of cases. Tumor attached to the pulmonary cusps or annulus and extended to adjacent tissues in all cases. Therefore, valve replacement or adjacent tissue reconstructions are required in 77% of cases. The recurrence and mortality are considerably high, with 33% and 22% cases, respectively. CONCLUSIONS: Pulmonary valve myxoma is more common in males with a bimodal age distribution, and its outcomes seem worse than usual cardiac myxomas. Increasing awareness of its clinical symptoms, early diagnosis, and complete myxoma resection before the presence of congestive heart failure symptoms are important in achieving excellent outcomes. A firm embolization blockade is needed to prevent myxoma recurrence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12957-023-02984-0. |
format | Online Article Text |
id | pubmed-10026419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100264192023-03-21 Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports Saputra, Pandit Bagus Tri Jannah, Ayik Rochyatul Rofananda, Ihsan Fahmi Al-Farabi, Makhyan Jibril Wungu, Citrawati Dyah Kencono Susilo, Hendri Alsagaff, Mochamad Yusuf Gusnanto, Arief Oktaviono, Yudi Her World J Surg Oncol Review BACKGROUND: Cardiac myxoma is the most common type of primary cardiac tumor, with the majority located in the atrial wall. The tumor is attached to valvular structures in a few cases, of which the pulmonary valve is the least affected. Pulmonary valve myxoma may have different clinical manifestations from the more common cardiac myxomas because of its vital position. A misdiagnosis of these types of cardiac myxoma may be detrimental to the care and well-being of patients. Therefore, this systematic review aims to define the clinical characteristics of pulmonary valve myxoma and how this differs from a more common cardiac myxoma. METHODS: Employed literature was obtained from PubMed, ScienceDirect, Scopus, Springer, and ProQuest without a publication year limit on August 23, 2022. The keyword was “pulmonary valve myxoma.” Inclusion criteria were as follows: (1) case report or series, (2) available individual patient data, and (3) myxoma that is attached to pulmonary valve structures with no evidence of metastasis. Non-English language or nonhuman subject studies were excluded. Johanna Briggs Institute checklists were used for the risk of bias assessment. Data are presented descriptively. RESULTS: This review included 9 case reports from 2237 articles. All cases show a low risk of bias. Pulmonary valve myxoma is dominated by males (5:4), and the patient’s median age is 57 years with a bimodal distribution in pediatric and geriatric populations. The clinical manifestation of pulmonary valve myxoma is often unspecified or asymptomatic. However, systolic murmur in the pulmonary valve area is heard in 67% of cases. Echocardiography remains the diagnostic modality of choice in the majority of cases. Tumor attached to the pulmonary cusps or annulus and extended to adjacent tissues in all cases. Therefore, valve replacement or adjacent tissue reconstructions are required in 77% of cases. The recurrence and mortality are considerably high, with 33% and 22% cases, respectively. CONCLUSIONS: Pulmonary valve myxoma is more common in males with a bimodal age distribution, and its outcomes seem worse than usual cardiac myxomas. Increasing awareness of its clinical symptoms, early diagnosis, and complete myxoma resection before the presence of congestive heart failure symptoms are important in achieving excellent outcomes. A firm embolization blockade is needed to prevent myxoma recurrence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12957-023-02984-0. BioMed Central 2023-03-20 /pmc/articles/PMC10026419/ /pubmed/36941612 http://dx.doi.org/10.1186/s12957-023-02984-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Saputra, Pandit Bagus Tri Jannah, Ayik Rochyatul Rofananda, Ihsan Fahmi Al-Farabi, Makhyan Jibril Wungu, Citrawati Dyah Kencono Susilo, Hendri Alsagaff, Mochamad Yusuf Gusnanto, Arief Oktaviono, Yudi Her Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
title | Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
title_full | Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
title_fullStr | Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
title_full_unstemmed | Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
title_short | Clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
title_sort | clinical characteristics, management, and outcomes of pulmonary valve myxoma: systematic review of published case reports |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026419/ https://www.ncbi.nlm.nih.gov/pubmed/36941612 http://dx.doi.org/10.1186/s12957-023-02984-0 |
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