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A case report of malignant primary pericardial mesothelioma with atypical imaging appearance: multimodality imaging with histopathological correlation
Abstract Background Primary pericardial mesothelioma is a rare primary cardiac malignancy, with three main histopathological types, sarcomatoid histotype being the rarest. The imaging features were atypical due to concomitant extensive calcification, which resulted in aggravated differential diagno...
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Published in: | European heart journal : case reports 2020-06, Vol.4 (2), p.1-5 |
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creator | Banišauskaitė, Audra Jankauskas, Antanas Šarauskas, Valdas Aržanauskaitė, Monika |
description | Abstract
Background
Primary pericardial mesothelioma is a rare primary cardiac malignancy, with three main histopathological types, sarcomatoid histotype being the rarest. The imaging features were atypical due to concomitant extensive calcification, which resulted in aggravated differential diagnosis.
Case summary
A 45-year-old man presented to our hospital with non-specific clinical symptoms. According to clinical history, a mediastinal tumour had been suspected with a previous unsuccessful attempt of transthoracic computed tomography-guided biopsy at an overseas hospital with limited data of performed imaging procedures. Multimodality imaging at our centre revealed extensively calcified solid masses in the pericardium, invading the left atrium. As the imaging features suggested an atypical primary pericardial malignancy, a diagnostic thoracoscopy was performed. Histopathological analysis of specimen revealed sarcomatoid type of pericardial mesothelioma with areas of necrosis and foci of osteogenic differentiation. Despite planned treatment, 2 weeks after histological diagnosis, the patient passed away due to perforated peptic ulcer-related sepsis.
Discussion
The presence of extensive calcification in the lesion resulted in a challenging imaging workup and diagnosis. Initial differential diagnosis included primary or metastatic calcification-prone tumour, secondary calcification due to haemorrhage after previous interventional procedure and other pathologies, such as tuberculous pericarditis, calcified amorphous tumour, among others. Calcification may be part of the histological tumour characteristics; however, proper history taking is crucial as concomitant diseases, previous treatment, and interventional procedures may alter the imaging pattern. |
doi_str_mv | 10.1093/ehjcr/ytaa034 |
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Background
Primary pericardial mesothelioma is a rare primary cardiac malignancy, with three main histopathological types, sarcomatoid histotype being the rarest. The imaging features were atypical due to concomitant extensive calcification, which resulted in aggravated differential diagnosis.
Case summary
A 45-year-old man presented to our hospital with non-specific clinical symptoms. According to clinical history, a mediastinal tumour had been suspected with a previous unsuccessful attempt of transthoracic computed tomography-guided biopsy at an overseas hospital with limited data of performed imaging procedures. Multimodality imaging at our centre revealed extensively calcified solid masses in the pericardium, invading the left atrium. As the imaging features suggested an atypical primary pericardial malignancy, a diagnostic thoracoscopy was performed. Histopathological analysis of specimen revealed sarcomatoid type of pericardial mesothelioma with areas of necrosis and foci of osteogenic differentiation. Despite planned treatment, 2 weeks after histological diagnosis, the patient passed away due to perforated peptic ulcer-related sepsis.
Discussion
The presence of extensive calcification in the lesion resulted in a challenging imaging workup and diagnosis. Initial differential diagnosis included primary or metastatic calcification-prone tumour, secondary calcification due to haemorrhage after previous interventional procedure and other pathologies, such as tuberculous pericarditis, calcified amorphous tumour, among others. Calcification may be part of the histological tumour characteristics; however, proper history taking is crucial as concomitant diseases, previous treatment, and interventional procedures may alter the imaging pattern.</description><identifier>ISSN: 2514-2119</identifier><identifier>EISSN: 2514-2119</identifier><identifier>DOI: 10.1093/ehjcr/ytaa034</identifier><identifier>PMID: 32352059</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Case Report</subject><ispartof>European heart journal : case reports, 2020-06, Vol.4 (2), p.1-5</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-5cc013509ac3111d936e8a8a2420c080cb498df26a1f09348619ad3cc924337c3</citedby><cites>FETCH-LOGICAL-c420t-5cc013509ac3111d936e8a8a2420c080cb498df26a1f09348619ad3cc924337c3</cites><orcidid>0000-0002-4695-485X ; 0000-0003-3784-5229 ; 0000-0002-4004-4150</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180536/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180536/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,1599,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32352059$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Santoro, Ciro</contributor><contributor>Vamvakidou, Anastasia</contributor><contributor>Aimo, Alberto</contributor><contributor>Patel, Peysh A.</contributor><contributor>Carlo, Marco De</contributor><creatorcontrib>Banišauskaitė, Audra</creatorcontrib><creatorcontrib>Jankauskas, Antanas</creatorcontrib><creatorcontrib>Šarauskas, Valdas</creatorcontrib><creatorcontrib>Aržanauskaitė, Monika</creatorcontrib><title>A case report of malignant primary pericardial mesothelioma with atypical imaging appearance: multimodality imaging with histopathological correlation</title><title>European heart journal : case reports</title><addtitle>Eur Heart J Case Rep</addtitle><description>Abstract
Background
Primary pericardial mesothelioma is a rare primary cardiac malignancy, with three main histopathological types, sarcomatoid histotype being the rarest. The imaging features were atypical due to concomitant extensive calcification, which resulted in aggravated differential diagnosis.
Case summary
A 45-year-old man presented to our hospital with non-specific clinical symptoms. According to clinical history, a mediastinal tumour had been suspected with a previous unsuccessful attempt of transthoracic computed tomography-guided biopsy at an overseas hospital with limited data of performed imaging procedures. Multimodality imaging at our centre revealed extensively calcified solid masses in the pericardium, invading the left atrium. As the imaging features suggested an atypical primary pericardial malignancy, a diagnostic thoracoscopy was performed. Histopathological analysis of specimen revealed sarcomatoid type of pericardial mesothelioma with areas of necrosis and foci of osteogenic differentiation. Despite planned treatment, 2 weeks after histological diagnosis, the patient passed away due to perforated peptic ulcer-related sepsis.
Discussion
The presence of extensive calcification in the lesion resulted in a challenging imaging workup and diagnosis. Initial differential diagnosis included primary or metastatic calcification-prone tumour, secondary calcification due to haemorrhage after previous interventional procedure and other pathologies, such as tuberculous pericarditis, calcified amorphous tumour, among others. Calcification may be part of the histological tumour characteristics; however, proper history taking is crucial as concomitant diseases, previous treatment, and interventional procedures may alter the imaging pattern.</description><subject>Case Report</subject><issn>2514-2119</issn><issn>2514-2119</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqFkU1v1DAQhi0Eaqu2x16Rj1xC_ZFkYw5IVQUFqRKXcramziRx5cTGdkD7R_p7cbfLUk6cbGkePzOel5ALzt5zpuQlTg8mXm4zAJP1K3IiGl5XgnP1-sX9mJyn9MAYE0yqdiOPyLEUshGsUSfk8YoaSEgjBh8z9QOdwdlxgSXTEO0McUsDRmsg9hYcnTH5PKGzfgb6y-aJQt6GUna0wKNdRgohIERYDH6g8-qynX1fnHl7IHbvJpuyD5An7_y4ExgfIzrI1i9n5M0ALuH5_jwl3z9_urv-Ut1-u_l6fXVbmVqwXDXGMC4bpsBIznmvZIsddCBK1bCOmftadf0gWuBD2VfdtVxBL41RopZyY-Qp-fjsDev9jL3BJUdwev9z7cHqfyuLnfTof-oN71gj2yJ4txdE_2PFlPVsk0HnYEG_Ji3KyrtG1rIpaPWMmuhTijgc2nCmn-LUuzj1Ps7Cv30524H-E97f3n4N_3H9BrnusFQ</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Banišauskaitė, Audra</creator><creator>Jankauskas, Antanas</creator><creator>Šarauskas, Valdas</creator><creator>Aržanauskaitė, Monika</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4695-485X</orcidid><orcidid>https://orcid.org/0000-0003-3784-5229</orcidid><orcidid>https://orcid.org/0000-0002-4004-4150</orcidid></search><sort><creationdate>20200601</creationdate><title>A case report of malignant primary pericardial mesothelioma with atypical imaging appearance: multimodality imaging with histopathological correlation</title><author>Banišauskaitė, Audra ; Jankauskas, Antanas ; Šarauskas, Valdas ; Aržanauskaitė, Monika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-5cc013509ac3111d936e8a8a2420c080cb498df26a1f09348619ad3cc924337c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Case Report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banišauskaitė, Audra</creatorcontrib><creatorcontrib>Jankauskas, Antanas</creatorcontrib><creatorcontrib>Šarauskas, Valdas</creatorcontrib><creatorcontrib>Aržanauskaitė, Monika</creatorcontrib><collection>Oxford University Press Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European heart journal : case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Banišauskaitė, Audra</au><au>Jankauskas, Antanas</au><au>Šarauskas, Valdas</au><au>Aržanauskaitė, Monika</au><au>Santoro, Ciro</au><au>Vamvakidou, Anastasia</au><au>Aimo, Alberto</au><au>Patel, Peysh A.</au><au>Carlo, Marco De</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case report of malignant primary pericardial mesothelioma with atypical imaging appearance: multimodality imaging with histopathological correlation</atitle><jtitle>European heart journal : case reports</jtitle><addtitle>Eur Heart J Case Rep</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>4</volume><issue>2</issue><spage>1</spage><epage>5</epage><pages>1-5</pages><issn>2514-2119</issn><eissn>2514-2119</eissn><abstract>Abstract
Background
Primary pericardial mesothelioma is a rare primary cardiac malignancy, with three main histopathological types, sarcomatoid histotype being the rarest. The imaging features were atypical due to concomitant extensive calcification, which resulted in aggravated differential diagnosis.
Case summary
A 45-year-old man presented to our hospital with non-specific clinical symptoms. According to clinical history, a mediastinal tumour had been suspected with a previous unsuccessful attempt of transthoracic computed tomography-guided biopsy at an overseas hospital with limited data of performed imaging procedures. Multimodality imaging at our centre revealed extensively calcified solid masses in the pericardium, invading the left atrium. As the imaging features suggested an atypical primary pericardial malignancy, a diagnostic thoracoscopy was performed. Histopathological analysis of specimen revealed sarcomatoid type of pericardial mesothelioma with areas of necrosis and foci of osteogenic differentiation. Despite planned treatment, 2 weeks after histological diagnosis, the patient passed away due to perforated peptic ulcer-related sepsis.
Discussion
The presence of extensive calcification in the lesion resulted in a challenging imaging workup and diagnosis. Initial differential diagnosis included primary or metastatic calcification-prone tumour, secondary calcification due to haemorrhage after previous interventional procedure and other pathologies, such as tuberculous pericarditis, calcified amorphous tumour, among others. Calcification may be part of the histological tumour characteristics; however, proper history taking is crucial as concomitant diseases, previous treatment, and interventional procedures may alter the imaging pattern.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>32352059</pmid><doi>10.1093/ehjcr/ytaa034</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-4695-485X</orcidid><orcidid>https://orcid.org/0000-0003-3784-5229</orcidid><orcidid>https://orcid.org/0000-0002-4004-4150</orcidid><oa>free_for_read</oa></addata></record> |
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title | A case report of malignant primary pericardial mesothelioma with atypical imaging appearance: multimodality imaging with histopathological correlation |
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