{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:18:56Z","timestamp":1787015936951,"version":"build-2736575974"},"reference-count":17,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2017,5,1]],"date-time":"2017-05-01T00:00:00Z","timestamp":1493596800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pathology International"],"published-print":{"date-parts":[[2017,6]]},"abstract":"\n \n Primary malignant pericardial sarcomatoid mesothelioma (PMPSM) is an extremely rare tumor with poor prognosis. We present an autopsy case in an 80\u2010year\u2010old man admitted for heart failure after one month of treatment at an outpatient clinic. He died three months after symptom onset. A complete autopsy revealed localization of the tumor to the pericardium without other lesions. Histologically, mainly spindle\u2010shaped atypical cells with hyperchromatic nuclei and nucleoli were observed. Immunohistochemical markers for mesothelioma were positive for calretinin, cytokeratin AE1\/AE3, and cytokeratin CAM5.2. Thus, we diagnosed primary sarcomatoid malignant mesothelioma of the pericardium. To our knowledge, only four PMPSM cases have been reported in the English literature in the past 30 years. Although PMPSM is rare, clinicians and pathologists should recognize it as a possible diagnosis of pericardial tumors. It is necessary to accumulate clinical and pathological diagnostic findings to establish early detection methods for this extremely rare disease.<\/jats:p>\n <\/jats:sec>","DOI":"10.1111\/pin.12535","type":"journal-article","created":{"date-parts":[[2017,5,2]],"date-time":"2017-05-02T11:14:41Z","timestamp":1493723681000},"page":"311-315","source":"Crossref","is-referenced-by-count":6,"title":["Primary malignant pericardial sarcomatoid mesothelioma: An autopsy report"],"prefix":"10.1111","volume":"67","author":[{"given":"Hiroko","family":"Muta","sequence":"first","affiliation":[{"name":"Department of Pathology Kurume University School of Medicine Kurume Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasuo","family":"Sugita","sequence":"additional","affiliation":[{"name":"Department of Pathology Kurume University School of Medicine Kurume Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Koichi","family":"Ohshima","sequence":"additional","affiliation":[{"name":"Department of Pathology Kurume University School of Medicine Kurume Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hitoshi","family":"Otsubo","sequence":"additional","affiliation":[{"name":"Oita Prefecture Saiseikai Hita Hospital Oita Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2017,5]]},"reference":[{"key":"e_1_2_6_2_1","volume-title":"WHO Classification of Tumors Pathology & Genetics of Tumors of the Lung, Pleura, Thymus and Heart","author":"Travis WD","year":"2004"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/s12199-007-0017-6"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1080\/00039890109604058"},{"key":"e_1_2_6_5_1","first-page":"1111","article-title":"Pathological study of diffuse malignant mesothelioma: A review of 117 cases collected by the Osaka mesothelioma Panel","volume":"17","author":"Sasaki M","year":"1999","journal-title":"Pathol Clin Med"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00432-010-0834-7"},{"key":"e_1_2_6_7_1","first-page":"170","article-title":"Primary malignant mesothelioma of the pericardium. 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