Rare Metastatic Mesothelioma Occupying Intra-Atrial Cavity, Released by an Emergency Surgery: A Case Report and Literature Review
INTRODUCTION: Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This report describes a case in which metastatic intracardiac mesothelioma triggered sudden respiratory failure, which was reduced by su...
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Published in | Surgical Case Reports Vol. 11; no. 1; p. cr.24-0176 |
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一般社団法人 日本外科学会 International Academic Publishing Co Ltd |
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Abstract | INTRODUCTION: Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This report describes a case in which metastatic intracardiac mesothelioma triggered sudden respiratory failure, which was reduced by surgical resection.CASE PRESENTATION: An 81-year-old man with a history of asbestos exposure presented to our hospital with sudden onset of dyspnea. Prior to this event, the pleura was involved in an epithelial malignancy, which was immunohistochemically negatively stained with anti-D2-40, WT-1, or anti-calretinin antibodies, which are positive markers of mesothelioma. Transthoracic echocardiography revealed a fragile and mobile tumor occupying the right atrium, and the patient was admitted for surgical tumorectomy. The operation was performed urgently using a cardiopulmonary bypass via a full sternotomy. The pericardium is grossly intact and does not adhere to the heart. A 3 × 5 cm tumor was tightly attached to the right atrium and was large enough to fit into the tricuspid valve. Therefore, the entire margin of the tumor stem attachment was resected from the lateral wall of the right atrium. Although the resected tumor was not positive for any of the three histopathological markers of mesothelioma, CDKN2A co-deletion revealed by fluorescence in situ hybridization led to a diagnosis of malignant mesothelioma.CONCLUSIONS: Surgical removal of intracardiac tumors that cause circulatory and respiratory instability is essential for the prevention of sudden death, regardless of prognostic determinants. This case demonstrates that mesotheliomas can metastasize to the endocardium. Even when nuclear atypia and negative results for immunohistochemical tests for the three mesothelioma markers suggest carcinoma, mesothelioma should still be considered and p16/CDKN2A co-deletion should be evaluated. |
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AbstractList | INTRODUCTION: Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This report describes a case in which metastatic intracardiac mesothelioma triggered sudden respiratory failure, which was reduced by surgical resection.CASE PRESENTATION: An 81-year-old man with a history of asbestos exposure presented to our hospital with sudden onset of dyspnea. Prior to this event, the pleura was involved in an epithelial malignancy, which was immunohistochemically negatively stained with anti-D2-40, WT-1, or anti-calretinin antibodies, which are positive markers of mesothelioma. Transthoracic echocardiography revealed a fragile and mobile tumor occupying the right atrium, and the patient was admitted for surgical tumorectomy. The operation was performed urgently using a cardiopulmonary bypass via a full sternotomy. The pericardium is grossly intact and does not adhere to the heart. A 3 × 5 cm tumor was tightly attached to the right atrium and was large enough to fit into the tricuspid valve. Therefore, the entire margin of the tumor stem attachment was resected from the lateral wall of the right atrium. Although the resected tumor was not positive for any of the three histopathological markers of mesothelioma, CDKN2A co-deletion revealed by fluorescence in situ hybridization led to a diagnosis of malignant mesothelioma.CONCLUSIONS: Surgical removal of intracardiac tumors that cause circulatory and respiratory instability is essential for the prevention of sudden death, regardless of prognostic determinants. This case demonstrates that mesotheliomas can metastasize to the endocardium. Even when nuclear atypia and negative results for immunohistochemical tests for the three mesothelioma markers suggest carcinoma, mesothelioma should still be considered and p16/CDKN2A co-deletion should be evaluated. Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This report describes a case in which metastatic intracardiac mesothelioma triggered sudden respiratory failure, which was reduced by surgical resection.INTRODUCTIONCardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This report describes a case in which metastatic intracardiac mesothelioma triggered sudden respiratory failure, which was reduced by surgical resection.An 81-year-old man with a history of asbestos exposure presented to our hospital with sudden onset of dyspnea. Prior to this event, the pleura was involved in an epithelial malignancy, which was immunohistochemically negatively stained with anti-D2-40, WT-1, or anti-calretinin antibodies, which are positive markers of mesothelioma. Transthoracic echocardiography revealed a fragile and mobile tumor occupying the right atrium, and the patient was admitted for surgical tumorectomy. The operation was performed urgently using a cardiopulmonary bypass via a full sternotomy. The pericardium is grossly intact and does not adhere to the heart. A 3 × 5 cm tumor was tightly attached to the right atrium and was large enough to fit into the tricuspid valve. Therefore, the entire margin of the tumor stem attachment was resected from the lateral wall of the right atrium. Although the resected tumor was not positive for any of the three histopathological markers of mesothelioma, CDKN2A co-deletion revealed by fluorescence in situ hybridization led to a diagnosis of malignant mesothelioma.CASE PRESENTATIONAn 81-year-old man with a history of asbestos exposure presented to our hospital with sudden onset of dyspnea. Prior to this event, the pleura was involved in an epithelial malignancy, which was immunohistochemically negatively stained with anti-D2-40, WT-1, or anti-calretinin antibodies, which are positive markers of mesothelioma. Transthoracic echocardiography revealed a fragile and mobile tumor occupying the right atrium, and the patient was admitted for surgical tumorectomy. The operation was performed urgently using a cardiopulmonary bypass via a full sternotomy. The pericardium is grossly intact and does not adhere to the heart. A 3 × 5 cm tumor was tightly attached to the right atrium and was large enough to fit into the tricuspid valve. Therefore, the entire margin of the tumor stem attachment was resected from the lateral wall of the right atrium. Although the resected tumor was not positive for any of the three histopathological markers of mesothelioma, CDKN2A co-deletion revealed by fluorescence in situ hybridization led to a diagnosis of malignant mesothelioma.Surgical removal of intracardiac tumors that cause circulatory and respiratory instability is essential for the prevention of sudden death, regardless of prognostic determinants. This case demonstrates that mesotheliomas can metastasize to the endocardium. Even when nuclear atypia and negative results for immunohistochemical tests for the three mesothelioma markers suggest carcinoma, mesothelioma should still be considered and p16/CDKN2A co-deletion should be evaluated.CONCLUSIONSSurgical removal of intracardiac tumors that cause circulatory and respiratory instability is essential for the prevention of sudden death, regardless of prognostic determinants. This case demonstrates that mesotheliomas can metastasize to the endocardium. Even when nuclear atypia and negative results for immunohistochemical tests for the three mesothelioma markers suggest carcinoma, mesothelioma should still be considered and p16/CDKN2A co-deletion should be evaluated. Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This report describes a case in which metastatic intracardiac mesothelioma triggered sudden respiratory failure, which was reduced by surgical resection. An 81-year-old man with a history of asbestos exposure presented to our hospital with sudden onset of dyspnea. Prior to this event, the pleura was involved in an epithelial malignancy, which was immunohistochemically negatively stained with anti-D2-40, WT-1, or anti-calretinin antibodies, which are positive markers of mesothelioma. Transthoracic echocardiography revealed a fragile and mobile tumor occupying the right atrium, and the patient was admitted for surgical tumorectomy. The operation was performed urgently using a cardiopulmonary bypass via a full sternotomy. The pericardium is grossly intact and does not adhere to the heart. A 3 × 5 cm tumor was tightly attached to the right atrium and was large enough to fit into the tricuspid valve. Therefore, the entire margin of the tumor stem attachment was resected from the lateral wall of the right atrium. Although the resected tumor was not positive for any of the three histopathological markers of mesothelioma, co-deletion revealed by fluorescence in situ hybridization led to a diagnosis of malignant mesothelioma. Surgical removal of intracardiac tumors that cause circulatory and respiratory instability is essential for the prevention of sudden death, regardless of prognostic determinants. This case demonstrates that mesotheliomas can metastasize to the endocardium. Even when nuclear atypia and negative results for immunohistochemical tests for the three mesothelioma markers suggest carcinoma, mesothelioma should still be considered and co-deletion should be evaluated. |
ArticleNumber | cr.24-0176 |
Author | Matsumura, Yu Kono, Tetsuya Takano, Tomohiro Ito, Ichiro Sato, Shuta Yamamoto, Manabu Tsukioka, Katsuaki |
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Cites_doi | 10.1007/s00059-016-4522-5 10.1136/jcp.2005.035105 10.1016/j.jtho.2019.08.2504 10.1159/000475491 10.1136/jitc-2019-000461 10.1093/jjco/hyaa069 10.15761/CCRR.1000414 10.1177/0003319706290737 10.1097/COC.0000000000001013 10.2486/indhealth.MS1184 10.1016/j.thorsurg.2010.12.001 10.1309/AJCPT94JVWIHBKRD |
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Keywords | cardiovascular oncologic emergencies p16/CDKN2A codeletion malignant mesothelioma metastatic cardiac tumor |
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References | 8) Kabbash MS, Edmund J, Ghafoor A, et al. Intracardiac involvement by primary malignant mesothelioma: a report of two cases. J Thorac Oncol 2020; 15: e25–7. 2) Senkottaiyan N, Seacord LM, Fulling KH, et al. Sarcomatous pleural mesothelioma metastatic to left ventricular endocardium: a case report and literature review. Angiology 2006; 57: 517–21. 3) Kopcik K, Kościelecka K, Krzyżak K. Cardiac metastatic tumors: current knowledge. Am J Clin Oncol 2023; 46: 374–9. 10) Jayaranagaiah A, Kariyanna PT, Chidella NKS, et al. Malignant pleural mesothelioma presenting with cardiac tamponade – a rare case report and review of the literature. Clin Case Rep Rev 2018; 4: 1000414. 5) Myojin T, Azuma K, Okumura J, et al. Future trends of mesothelioma mortality in Japan based on a risk function. Ind Health 2012; 50: 197–204. 7) Hotta K, Fujimoto N. Current evidence and future perspectives of immune-checkpoint inhibitors in unresectable malignant pleural mesothelioma. J Immunother Cancer 2020; 8: e000461. 12) Shenoy S, Shetty S, Lankala S, et al. Cardiovascular oncologic emergencies. Cardiology 2017; 138: 147–58. 1) Cao S, Jin S, Cao J, et al. Malignant pericardial mesothelioma: a systematic review of current practice. Herz 2018; 43: 61–8. 4) Wu D, Hiroshima K, Matsumoto S, et al. Diagnostic usefulness of p16/CDKN2A FISH in distinguishing between sarcomatoid mesothelioma and fibrous pleuritis. Am J Clin Pathol 2013; 139: 39–46. 9) Bussani R, De-Giorgio F, Abbate A, et al. Cardiac metastases. J Clin Pathol 2007; 60: 27–34. 6) Nakamura A, Kondo N, Nakamichi T, et al. Initial evaluation of nivolumab in patients with post-operative recurrence of malignant pleural mesothelioma. Jpn J Clin Oncol 2020; 50: 920–5. 11) Finley DJ, Rusch VW. Anatomy of the pleura. Thorac Surg Clin 2011; 21: 157–63. 11 1 12 2 3 4 5 6 7 8 9 10 |
References_xml | – reference: 4) Wu D, Hiroshima K, Matsumoto S, et al. Diagnostic usefulness of p16/CDKN2A FISH in distinguishing between sarcomatoid mesothelioma and fibrous pleuritis. Am J Clin Pathol 2013; 139: 39–46. – reference: 10) Jayaranagaiah A, Kariyanna PT, Chidella NKS, et al. Malignant pleural mesothelioma presenting with cardiac tamponade – a rare case report and review of the literature. Clin Case Rep Rev 2018; 4: 1000414. – reference: 6) Nakamura A, Kondo N, Nakamichi T, et al. Initial evaluation of nivolumab in patients with post-operative recurrence of malignant pleural mesothelioma. Jpn J Clin Oncol 2020; 50: 920–5. – reference: 12) Shenoy S, Shetty S, Lankala S, et al. Cardiovascular oncologic emergencies. Cardiology 2017; 138: 147–58. – reference: 1) Cao S, Jin S, Cao J, et al. Malignant pericardial mesothelioma: a systematic review of current practice. Herz 2018; 43: 61–8. – reference: 2) Senkottaiyan N, Seacord LM, Fulling KH, et al. Sarcomatous pleural mesothelioma metastatic to left ventricular endocardium: a case report and literature review. Angiology 2006; 57: 517–21. – reference: 7) Hotta K, Fujimoto N. Current evidence and future perspectives of immune-checkpoint inhibitors in unresectable malignant pleural mesothelioma. J Immunother Cancer 2020; 8: e000461. – reference: 5) Myojin T, Azuma K, Okumura J, et al. Future trends of mesothelioma mortality in Japan based on a risk function. Ind Health 2012; 50: 197–204. – reference: 8) Kabbash MS, Edmund J, Ghafoor A, et al. Intracardiac involvement by primary malignant mesothelioma: a report of two cases. J Thorac Oncol 2020; 15: e25–7. – reference: 11) Finley DJ, Rusch VW. Anatomy of the pleura. Thorac Surg Clin 2011; 21: 157–63. – reference: 3) Kopcik K, Kościelecka K, Krzyżak K. Cardiac metastatic tumors: current knowledge. Am J Clin Oncol 2023; 46: 374–9. – reference: 9) Bussani R, De-Giorgio F, Abbate A, et al. Cardiac metastases. J Clin Pathol 2007; 60: 27–34. – ident: 1 doi: 10.1007/s00059-016-4522-5 – ident: 9 doi: 10.1136/jcp.2005.035105 – ident: 8 doi: 10.1016/j.jtho.2019.08.2504 – ident: 12 doi: 10.1159/000475491 – ident: 7 doi: 10.1136/jitc-2019-000461 – ident: 6 doi: 10.1093/jjco/hyaa069 – ident: 10 doi: 10.15761/CCRR.1000414 – ident: 2 doi: 10.1177/0003319706290737 – ident: 3 doi: 10.1097/COC.0000000000001013 – ident: 5 doi: 10.2486/indhealth.MS1184 – ident: 11 doi: 10.1016/j.thorsurg.2010.12.001 – ident: 4 doi: 10.1309/AJCPT94JVWIHBKRD |
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Snippet | INTRODUCTION: Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain... Cardiac surgery for cardiovascular-associated mesothelioma has a poor prognosis. However, life-saving surgery is unavoidable to maintain circulation. This... |
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SubjectTerms | Biopsy Cancer therapies cardiovascular oncologic emergencies Case Report Chemotherapy Dyspnea Heart surgery Immune checkpoint inhibitors Intensive care Lung cancer malignant mesothelioma Mesothelioma Metastasis metastatic cardiac tumor p16/CDKN2A codeletion Peptides Tomography Tumors |
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Title | Rare Metastatic Mesothelioma Occupying Intra-Atrial Cavity, Released by an Emergency Surgery: A Case Report and Literature Review |
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ispartofPNX | Surgical Case Reports, 2025, Vol.11(1), pp.cr.24-0176 |
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