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Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas
BACKGROUND: Pediatric primary cardiac tumors (PCTs) are rare. Its clinical features and prognoses are not well defined. The management of asymptomatic patients with cardiac fibromas remains controversial. OBJECTIVE: We aimed to examine our experience in surgical resection of pediatric PCT, with spec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934860/ https://www.ncbi.nlm.nih.gov/pubmed/35321111 http://dx.doi.org/10.3389/fcvm.2022.808394 |
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author | Qian, Tao Wu, Zhongshi Yang, Yifeng Xie, Li Yin, Ni Lu, Ting Huang, Can Yang, Hui |
author_facet | Qian, Tao Wu, Zhongshi Yang, Yifeng Xie, Li Yin, Ni Lu, Ting Huang, Can Yang, Hui |
author_sort | Qian, Tao |
collection | PubMed |
description | BACKGROUND: Pediatric primary cardiac tumors (PCTs) are rare. Its clinical features and prognoses are not well defined. The management of asymptomatic patients with cardiac fibromas remains controversial. OBJECTIVE: We aimed to examine our experience in surgical resection of pediatric PCT, with specific focuses on the management of large fibromas. METHODS: This study included all the children who underwent surgical resection of PCT in our institution between December 2008 and June 2021. The last follow-up was performed between June 1st and August 26th, 2021. Kaplan–Meier method was used to estimate the postoperative survival, freedom from reoperation, event-free survival, and also related risk factors. The tumor volume and volume index (volume divided by body surface area) were measured for cardiac fibromas. RESULTS: Of the 39 patients with median operative age of 9.5 [interquartile range (IQR): 1.2–16.5] years, 35 (89.7%) had benign tumors (fibromas for 15, myxomas for 13, and others for 7). The length and volume of fibromas were independent of age and symptoms (Ps > 0.05). The fibroma volume index was negatively correlated with age (P = 0.039), with a mean value of 105 ± 70 ml/m(2). Of the 15 patients with fibromas, 5 were asymptomatic, 4 received partial resection, 4 required transmural resection, and 4 presented postoperative left ventricular (LV) dysfunction (ejection fraction <50%). During the median follow-up period of 3.1 years and maximum of 12.5 years, adverse events included 2 early and 1 late death, 4 reoperations, 4 tumor recurrences, and 1 LV dysfunction lasting over one year. The 8-year survival, freedom from reoperation, and event-free survival rates were 90.4, 81.8, and 64.2%, respectively. Malignant tumor (P < 0.001) was associated with more adverse events. Transmural resection (P = 0.022) and larger tumor volume index than LV end-diastolic volume (P = 0.046) were risk factors for LV dysfunction following fibromas resection. CONCLUSION: Pediatric surgery for PCT can be performed with low mortalities and few adverse events. The size of cardiac fibroma in children relatively decreases with the increase of age. Larger tumor volume index than LV end-diastolic volume index and transmural tumor resection predicts postoperative LV dysfunction. |
format | Online Article Text |
id | pubmed-8934860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89348602022-03-22 Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas Qian, Tao Wu, Zhongshi Yang, Yifeng Xie, Li Yin, Ni Lu, Ting Huang, Can Yang, Hui Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Pediatric primary cardiac tumors (PCTs) are rare. Its clinical features and prognoses are not well defined. The management of asymptomatic patients with cardiac fibromas remains controversial. OBJECTIVE: We aimed to examine our experience in surgical resection of pediatric PCT, with specific focuses on the management of large fibromas. METHODS: This study included all the children who underwent surgical resection of PCT in our institution between December 2008 and June 2021. The last follow-up was performed between June 1st and August 26th, 2021. Kaplan–Meier method was used to estimate the postoperative survival, freedom from reoperation, event-free survival, and also related risk factors. The tumor volume and volume index (volume divided by body surface area) were measured for cardiac fibromas. RESULTS: Of the 39 patients with median operative age of 9.5 [interquartile range (IQR): 1.2–16.5] years, 35 (89.7%) had benign tumors (fibromas for 15, myxomas for 13, and others for 7). The length and volume of fibromas were independent of age and symptoms (Ps > 0.05). The fibroma volume index was negatively correlated with age (P = 0.039), with a mean value of 105 ± 70 ml/m(2). Of the 15 patients with fibromas, 5 were asymptomatic, 4 received partial resection, 4 required transmural resection, and 4 presented postoperative left ventricular (LV) dysfunction (ejection fraction <50%). During the median follow-up period of 3.1 years and maximum of 12.5 years, adverse events included 2 early and 1 late death, 4 reoperations, 4 tumor recurrences, and 1 LV dysfunction lasting over one year. The 8-year survival, freedom from reoperation, and event-free survival rates were 90.4, 81.8, and 64.2%, respectively. Malignant tumor (P < 0.001) was associated with more adverse events. Transmural resection (P = 0.022) and larger tumor volume index than LV end-diastolic volume (P = 0.046) were risk factors for LV dysfunction following fibromas resection. CONCLUSION: Pediatric surgery for PCT can be performed with low mortalities and few adverse events. The size of cardiac fibroma in children relatively decreases with the increase of age. Larger tumor volume index than LV end-diastolic volume index and transmural tumor resection predicts postoperative LV dysfunction. Frontiers Media S.A. 2022-03-07 /pmc/articles/PMC8934860/ /pubmed/35321111 http://dx.doi.org/10.3389/fcvm.2022.808394 Text en Copyright © 2022 Qian, Wu, Yang, Xie, Yin, Lu, Huang and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Qian, Tao Wu, Zhongshi Yang, Yifeng Xie, Li Yin, Ni Lu, Ting Huang, Can Yang, Hui Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas |
title | Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas |
title_full | Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas |
title_fullStr | Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas |
title_full_unstemmed | Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas |
title_short | Surgery for Primary Cardiac Tumors in Children: Successful Management of Large Fibromas |
title_sort | surgery for primary cardiac tumors in children: successful management of large fibromas |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934860/ https://www.ncbi.nlm.nih.gov/pubmed/35321111 http://dx.doi.org/10.3389/fcvm.2022.808394 |
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