Multimodal imaging features of primary pericardial synovial sarcoma: a case report
Primary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in the literature.BackgroundPrimary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognos...
Saved in:
Published in | Frontiers in oncology Vol. 13; p. 1181778 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
04.08.2023
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Primary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in the literature.BackgroundPrimary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in the literature.A 34-year-old man was admitted to our hospital with chest tightness and a cough. An echocardiogram revealed a heterogeneous mass with a large pericardial effusion. Further computed tomography (CT) of the chest and cardiac magnetic resonance imaging (CMRI) demonstrated an irregular pericardial mass abutting the left atrium and left ventricle and invading the mediastinal structures. Pathology results showed that the tumor was a monophasic synovial sarcoma. The patient underwent chemotherapy and survived for 17 months.Case summaryA 34-year-old man was admitted to our hospital with chest tightness and a cough. An echocardiogram revealed a heterogeneous mass with a large pericardial effusion. Further computed tomography (CT) of the chest and cardiac magnetic resonance imaging (CMRI) demonstrated an irregular pericardial mass abutting the left atrium and left ventricle and invading the mediastinal structures. Pathology results showed that the tumor was a monophasic synovial sarcoma. The patient underwent chemotherapy and survived for 17 months.Many cardiac tumors are clinically asymptomatic or nonspecific, and they are frequently detected or diagnosed at an advanced stage of the disease. Multimodal cardiac imaging facilitates the detection and assessment of cardiac tumors. In particular, CMRI is considered as a superior imaging tool, because it provides high tissue contrast and can detect invasion of the myocardium. We describe the clinical details and multimodal imaging features of a rare primary pericardial synovial sarcoma, hoping to provide guidance for the diagnosis of similar cases in the future.DiscussionMany cardiac tumors are clinically asymptomatic or nonspecific, and they are frequently detected or diagnosed at an advanced stage of the disease. Multimodal cardiac imaging facilitates the detection and assessment of cardiac tumors. In particular, CMRI is considered as a superior imaging tool, because it provides high tissue contrast and can detect invasion of the myocardium. We describe the clinical details and multimodal imaging features of a rare primary pericardial synovial sarcoma, hoping to provide guidance for the diagnosis of similar cases in the future. |
---|---|
AbstractList | BackgroundPrimary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in the literature.Case summaryA 34-year-old man was admitted to our hospital with chest tightness and a cough. An echocardiogram revealed a heterogeneous mass with a large pericardial effusion. Further computed tomography (CT) of the chest and cardiac magnetic resonance imaging (CMRI) demonstrated an irregular pericardial mass abutting the left atrium and left ventricle and invading the mediastinal structures. Pathology results showed that the tumor was a monophasic synovial sarcoma. The patient underwent chemotherapy and survived for 17 months.DiscussionMany cardiac tumors are clinically asymptomatic or nonspecific, and they are frequently detected or diagnosed at an advanced stage of the disease. Multimodal cardiac imaging facilitates the detection and assessment of cardiac tumors. In particular, CMRI is considered as a superior imaging tool, because it provides high tissue contrast and can detect invasion of the myocardium. We describe the clinical details and multimodal imaging features of a rare primary pericardial synovial sarcoma, hoping to provide guidance for the diagnosis of similar cases in the future. Primary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in the literature.BackgroundPrimary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in the literature.A 34-year-old man was admitted to our hospital with chest tightness and a cough. An echocardiogram revealed a heterogeneous mass with a large pericardial effusion. Further computed tomography (CT) of the chest and cardiac magnetic resonance imaging (CMRI) demonstrated an irregular pericardial mass abutting the left atrium and left ventricle and invading the mediastinal structures. Pathology results showed that the tumor was a monophasic synovial sarcoma. The patient underwent chemotherapy and survived for 17 months.Case summaryA 34-year-old man was admitted to our hospital with chest tightness and a cough. An echocardiogram revealed a heterogeneous mass with a large pericardial effusion. Further computed tomography (CT) of the chest and cardiac magnetic resonance imaging (CMRI) demonstrated an irregular pericardial mass abutting the left atrium and left ventricle and invading the mediastinal structures. Pathology results showed that the tumor was a monophasic synovial sarcoma. The patient underwent chemotherapy and survived for 17 months.Many cardiac tumors are clinically asymptomatic or nonspecific, and they are frequently detected or diagnosed at an advanced stage of the disease. Multimodal cardiac imaging facilitates the detection and assessment of cardiac tumors. In particular, CMRI is considered as a superior imaging tool, because it provides high tissue contrast and can detect invasion of the myocardium. We describe the clinical details and multimodal imaging features of a rare primary pericardial synovial sarcoma, hoping to provide guidance for the diagnosis of similar cases in the future.DiscussionMany cardiac tumors are clinically asymptomatic or nonspecific, and they are frequently detected or diagnosed at an advanced stage of the disease. Multimodal cardiac imaging facilitates the detection and assessment of cardiac tumors. In particular, CMRI is considered as a superior imaging tool, because it provides high tissue contrast and can detect invasion of the myocardium. We describe the clinical details and multimodal imaging features of a rare primary pericardial synovial sarcoma, hoping to provide guidance for the diagnosis of similar cases in the future. |
Author | Jin, Hongrui Zhang, Wenbo Wang, Keyan Zhang, Yong |
AuthorAffiliation | Department of Magnetic Resonance Imaging, The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China |
AuthorAffiliation_xml | – name: Department of Magnetic Resonance Imaging, The First Affiliated Hospital of Zhengzhou University , Zhengzhou , China |
Author_xml | – sequence: 1 givenname: Hongrui surname: Jin fullname: Jin, Hongrui – sequence: 2 givenname: Yong surname: Zhang fullname: Zhang, Yong – sequence: 3 givenname: Wenbo surname: Zhang fullname: Zhang, Wenbo – sequence: 4 givenname: Keyan surname: Wang fullname: Wang, Keyan |
BookMark | eNpVkctqFEEUhguJYIx5AHe9dDNj3S9uRIKXQIIgCu6K01WnxgrdXWNVdyBvb09mkORszpXv_PC_JmdTmZCQt4xuhbDufSpT2HLKxZYxy4yxL8g550JunBS_z57Ur8hla3d0Da0oo-Kc_LhdhjmPJcLQ5RF2edp1CWFeKraupG5f12l96PZYc4Aa83rXHqZy_1hADWWEDx10ARp2Ffelzm_IywRDw8tTviC_vnz-efVtc_P96_XVp5tNEE7NG5VkElKZKANPLHIRknF94NoqqoWM2loRgzKUORdE0IZBTDqiEoiJKy0uyPWRGwvc-ZNQXyD7x0GpOw91zmFAr2VvQnAK0aI0GgBw7VIU0fWqh7iyPh5Z-6UfMQac5grDM-jzzZT_-F2594xKoaVxK-HdiVDL3wXb7MfcAg4DTFiW5rlVUkir-UE4O56GWlqrmP7_YdQfDPUHQ_3BUH8yVPwDFqGY-g |
Cites_doi | 10.1002/(SICI)1096-9098(199903)70:3<194::AID-JSO10>3.0.CO;2-8 10.3969/j.issn.1002-1671.2013.01.023 10.1055/s-0039-1692409 10.1016/j.anndiagpath.2014.09.002 10.1177/0218492319873822 10.3969/j.issn.1007-5410.2013.04.019 10.1111/jocs.14214 10.1200/JCO.2004.11.093 10.1016/j.athoracsur.2013.01.030 10.1016/0003-4975(91)91003-E 10.1007/s00595-013-0720-4 10.1134/S0026893311040078 10.1309/AJCP34ZVFLAUTMGL 10.1016/S0300-8932(03)76886-9 10.1016/j.carpath.2020.107286 |
ContentType | Journal Article |
Copyright | Copyright © 2023 Jin, Zhang, Zhang and Wang. Copyright © 2023 Jin, Zhang, Zhang and Wang 2023 Jin, Zhang, Zhang and Wang |
Copyright_xml | – notice: Copyright © 2023 Jin, Zhang, Zhang and Wang. – notice: Copyright © 2023 Jin, Zhang, Zhang and Wang 2023 Jin, Zhang, Zhang and Wang |
DBID | AAYXX CITATION 7X8 5PM DOA |
DOI | 10.3389/fonc.2023.1181778 |
DatabaseName | CrossRef MEDLINE - Academic PubMed Central (Full Participant titles) Directory of Open Access Journals (DOAJ) |
DatabaseTitle | CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 2234-943X |
ExternalDocumentID | oai_doaj_org_article_64b7cc95ee8e476aaaec95fd3d9b5bad PMC10436479 10_3389_fonc_2023_1181778 |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK EBS EJD EMOBN GROUPED_DOAJ GX1 HYE KQ8 M48 M~E OK1 PGMZT RNS RPM 7X8 5PM |
ID | FETCH-LOGICAL-c395t-5f4f3457d4c2f1d23cf79bc26850634d6883dc570199c3c671adf6de53eef2563 |
IEDL.DBID | M48 |
ISSN | 2234-943X |
IngestDate | Wed Aug 27 01:27:54 EDT 2025 Thu Aug 21 18:40:29 EDT 2025 Fri Jul 11 09:02:02 EDT 2025 Tue Jul 01 02:58:22 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Language | English |
License | 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. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c395t-5f4f3457d4c2f1d23cf79bc26850634d6883dc570199c3c671adf6de53eef2563 |
Notes | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 Reviewed by: Massimo Baudo, Spedali Civili Brescia, Italy; Jing Ping Sun, Cleveland Clinic, United States Edited by: Mingxing Xie, Huazhong University of Science and Technology, China |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fonc.2023.1181778 |
PQID | 2854348626 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_64b7cc95ee8e476aaaec95fd3d9b5bad pubmedcentral_primary_oai_pubmedcentral_nih_gov_10436479 proquest_miscellaneous_2854348626 crossref_primary_10_3389_fonc_2023_1181778 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-08-04 |
PublicationDateYYYYMMDD | 2023-08-04 |
PublicationDate_xml | – month: 08 year: 2023 text: 2023-08-04 day: 04 |
PublicationDecade | 2020 |
PublicationTitle | Frontiers in oncology |
PublicationYear | 2023 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Kekeeva (B6) 2011; 45 Coli (B13) 2019; 34 Zhang (B9) 2011; 18 Jiménez Mazuecos (B16) 2003; 56 Teng (B7) 2021; 50 Ren (B11) 2013; 18 Huang (B12) 2013; 29 Yoshino (B5) 2014; 44 Huang (B10) 2016; 26 Al-Rajhi (B15) 1999; 70 Guillou (B4) 2004; 22 Wong (B17) 2020; 28 Aboud (B3) 2019; 67 Putnam (B14) 1991; 51 Thway (B1) 2014; 18 Wang (B2) 2013; 95 Cheng (B8) 2012; 137 |
References_xml | – volume: 70 year: 1999 ident: B15 article-title: Primary pericardial synovial sarcoma: a case report and literature review publication-title: J Surg Oncol doi: 10.1002/(SICI)1096-9098(199903)70:3<194::AID-JSO10>3.0.CO;2-8 – volume: 29 start-page: 88 year: 2013 ident: B12 article-title: CT and MRI findings of synovial sarcoma of soft tissue publication-title: J Pract Radiol doi: 10.3969/j.issn.1002-1671.2013.01.023 – volume: 67 year: 2019 ident: B3 article-title: Prognostic factors for long-term survival after surgical resection of primary cardiac sarcoma publication-title: Thorac Cardiovasc Surg doi: 10.1055/s-0039-1692409 – volume: 18 year: 2011 ident: B9 article-title: Primary synovial sarcoma of the heart publication-title: Cardiol J – volume: 18 year: 2014 ident: B1 article-title: Synovial sarcoma: defining features and diagnostic evolution publication-title: Ann Diagn Pathol doi: 10.1016/j.anndiagpath.2014.09.002 – volume: 28 start-page: 59 year: 2020 ident: B17 article-title: Pericardial synovial sarcoma presenting with unstable angina publication-title: Asian Cardiovasc Thorac Ann doi: 10.1177/0218492319873822 – volume: 18 year: 2013 ident: B11 article-title: Primary synovial sarcoma of the left ventricle: a case report publication-title: Chin J Cardiovasc Med doi: 10.3969/j.issn.1007-5410.2013.04.019 – volume: 34 year: 2019 ident: B13 article-title: Primary cardiac synovial sarcoma: a review correlating outcomes with surgery and adjuvant therapy publication-title: J Card Surg doi: 10.1111/jocs.14214 – volume: 22 year: 2004 ident: B4 article-title: Histologic grade, but not SYT-SSX fusion type, is an important prognostic factor in patients with synovial sarcoma: a multicenter, retrospective analysis publication-title: J Clin Oncol doi: 10.1200/JCO.2004.11.093 – volume: 95 year: 2013 ident: B2 article-title: Primary cardiac synovial sarcoma publication-title: Ann Thorac Surg doi: 10.1016/j.athoracsur.2013.01.030 – volume: 26 year: 2016 ident: B10 article-title: CT and MRI findings of synovial sarcoma publication-title: J Med Imaging (Bellingham) – volume: 51 year: 1991 ident: B14 article-title: Primary cardiac sarcomas publication-title: Ann Thorac Surg doi: 10.1016/0003-4975(91)91003-E – volume: 44 year: 2014 ident: B5 article-title: Pericardial synovial sarcoma: a case report and review of the literature publication-title: Surg Today doi: 10.1007/s00595-013-0720-4 – volume: 45 year: 2011 ident: B6 article-title: Analysis of SYT/SSX1 and SYT/SSX2 fusion genes from synovial sarcoma publication-title: Mol Biol doi: 10.1134/S0026893311040078 – volume: 137 year: 2012 ident: B8 article-title: Pericardial synovial sarcoma, a potential for misdiagnosis: clinicopathologic and molecular cytogenetic analysis of three cases with literature review publication-title: Am J Clin Pathol doi: 10.1309/AJCP34ZVFLAUTMGL – volume: 56 year: 2003 ident: B16 article-title: Rivera LAP Is heart transplantation for primary cardiac sarcoma a useful therapeutic option publication-title: Rev Esp Cardiol doi: 10.1016/S0300-8932(03)76886-9 – volume: 50 year: 2021 ident: B7 article-title: Primary cardiac synovial sarcoma: a clinicopathological, immunohistochemical, and molecular genetics study of five clinical cases publication-title: Cardiovasc Pathol doi: 10.1016/j.carpath.2020.107286 |
SSID | ssj0000650103 |
Score | 2.3174956 |
Snippet | Primary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been reported in... BackgroundPrimary pericardial synovial sarcoma is an extremely rare malignant tumor, and affected patients have a poor prognosis. Only a few cases have been... |
SourceID | doaj pubmedcentral proquest crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database |
StartPage | 1181778 |
SubjectTerms | cardiac magnetic resonance imaging computed tomography echocardiogram multimodal imaging Oncology pericardial synovial sarcoma |
SummonAdditionalLinks | – databaseName: Directory of Open Access Journals (DOAJ) dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1LSwMxEA7Sg3gRn1hfRPAkrGWbZLPxpmIpQj2Ihd5CNg8s2N1iW8F_70x2K92TF0_7hE1mhplvdpJvCLlmAIlzgBWJADCbcK_ADzIjE-eVtbkJcMRfA6OXbDjmzxMx2Wj1hWvCanrgWnC9jBfSWiW8zz2XmTHGw1VwzKlCFMah94WYt5FM1T5YYAODuowJWZjqhapExsI-u8WtlhLbqm0EosjX3wKZ7SWSGzFnsEd2G7BI7-tB7pMtXx6Q7VFTDj8kr3H77Kxy8NJ0FvsN0eAjVeeCVoHOayoJOo9VGTSFD7r4LquveAImXs3MHTXUQiijdfXgiIwHT2-Pw6RpkpBYpsQyEYEHxoV03PZD6vrMBqkK28-Qio5xl-U5c1Yg67qyzGYyNS5kzgvmfQC8w45Jp6xKf0Iod6m1qQMIJgw3HLsdyMwFcICeBZB3l9ysJaabCWjIIVC8GsWrUby6EW-XPKBMf19EGut4A5SrG-Xqv5TbJVdrjWgwe6xlmNJXq4XGjZ-MYzrWJXlLVa0vtp-U0_dIoJ0i7z6X6vQ_xnhGdnDecVEgPyed5efKXwBQWRaX0SZ_ALAa7AE priority: 102 providerName: Directory of Open Access Journals |
Title | Multimodal imaging features of primary pericardial synovial sarcoma: a case report |
URI | https://www.proquest.com/docview/2854348626 https://pubmed.ncbi.nlm.nih.gov/PMC10436479 https://doaj.org/article/64b7cc95ee8e476aaaec95fd3d9b5bad |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1La9wwEB6SFEIupY-EbB9BhZwCTrAlWVaglLY0DYXNIXRhb0LWI1nI2snupjT_PjOyN9SQSy-2ZRsLjTSabzzSNwCHHCFxhbAikwhmMxE0zoPcqswH7VxlI57p18D4ojyfiF9TOd2AdXqrXoDLZ107yic1Wdwc_717-IIK_5k8TrS3J7FtiIyw4Me0i1KpahNeoGFSlNBg3KP9bmKWlNWA0s0VXGRa8GkX53z-KwNLlQj9Byh0uIbyH6N09gpe9miSfe26_zVshOYNbI_7ePlbuEz7a-etx5dm85SQiMWQuDyXrI3stuOaYLcpbENj5YYtH5r2T7pAHWjn9pRZ5tDWsS68sAuTsx-_v59nfRaFzHEtV5mMInIhlReuiLkvuItK164oiauOC19WFfdOEi27dtyVKrc-lj5IHkJEQMT3YKtpm7APTPjcudwjRpNWWEHpEFTpI86QgUfu9QiO1hIzfQMMOhkkXkPiNSRe04t3BN9Ipk8vEs91utEurkyvNqYUtXJOyxCqIFRprQ1Yih4rq2Vt_Qg-rXvEoF5QsMM2ob1fGtoZygX5ayOoBl01qHH4pJldJ4btnIj5hdLv_qdB72GHiml1oPgAW6vFffiIiGVVHyRPH48_p_lBGpOPJ7Hspg |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Multimodal+imaging+features+of+primary+pericardial+synovial+sarcoma%3A+a+case+report&rft.jtitle=Frontiers+in+oncology&rft.au=Jin%2C+Hongrui&rft.au=Zhang%2C+Yong&rft.au=Zhang%2C+Wenbo&rft.au=Wang%2C+Keyan&rft.date=2023-08-04&rft.issn=2234-943X&rft.eissn=2234-943X&rft.volume=13&rft_id=info:doi/10.3389%2Ffonc.2023.1181778&rft.externalDBID=n%2Fa&rft.externalDocID=10_3389_fonc_2023_1181778 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2234-943X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2234-943X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2234-943X&client=summon |