2020
DOI: 10.1016/j.ijscr.2020.07.054
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Primary malignant pericardial mesothelioma presenting with cardiac tamponade

Abstract: Highlights Primary malignant pericardial mesothelioma is rare, and its diagnosis is difficult. The surgical intervention was performed after pericardiocentesis for definitive diagnosis and treatment. The prognosis of malignant pericardial mesothelioma was very poor. The indications for surgical intervention should be carefully considered except for critical cases.

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Cited by 5 publications
(4 citation statements)
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“…Pericardial malignant mesotheliomas are relatively rare malignant cardiac tumors, which are often associated with excessive pericardial effusion or tamponade ( Figure 5I1,5I2 ) ( 32 , 33 ). The disease has a poor prognosis, and patients have a short life expectancy ( 33 ).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Pericardial malignant mesotheliomas are relatively rare malignant cardiac tumors, which are often associated with excessive pericardial effusion or tamponade ( Figure 5I1,5I2 ) ( 32 , 33 ). The disease has a poor prognosis, and patients have a short life expectancy ( 33 ).…”
Section: Discussionmentioning
confidence: 99%
“…Pericardial malignant mesotheliomas are relatively rare malignant cardiac tumors, which are often associated with excessive pericardial effusion or tamponade ( Figure 5I1,5I2 ) ( 32 , 33 ). The disease has a poor prognosis, and patients have a short life expectancy ( 33 ). In our study, 1 patient with malignant pericardial mesothelioma survived for 52 months after undergoing a partial resection of the tumor body combined with radiotherapy and chemotherapy.…”
Section: Discussionmentioning
confidence: 99%
“…Surgery is the most important treatment. The operation includes pericardiectomy and pericardial window placement [Matsuyama 2020]. It is mostly useful for preventing cardiac tamponade or reducing tumor.…”
Section: Discussionmentioning
confidence: 99%
“…Primary malignant pericardial mesothelioma (PPM) is a malignant heart tumor originating in the serous pericardium and is highly invasive 1,2 . Through the collection of clinical data from a patient with PPM and literature review, the clinical manifestations, diagnostic methods, treatment and prognosis, pathological results and immunohistochemical characteristics of PPM are further discussed to expand the understanding of the disease and improve its diagnosis and treatment.…”
Section: Introductionmentioning
confidence: 99%