Related Experiment Video
Updated: Dec 13, 2025

Generation and Expansion of Primary, Malignant Pleural Mesothelioma Tumor Lines
Published on: April 21, 2022
Primary malignant pericardial mesothelioma presenting with cardiac tamponade
Shigefumi Matsuyama1, Tomohiro Imazuru2, Masateru Uchiyama2
1Department of Cardiovascular Surgery, Toranomon Hospital, 2-2-2 Toranomon, Minato-ku, Tokyo, 105-8470, Japan; Department of Cardiovascular Surgery, Teikyo University Hospital, 2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8606, Japan.
Introduction:
Primary malignant pericardial mesothelioma is a rare tumor that is very difficult to diagnose. Furthermore, it is a lethal disease, because patients usually have progressed at the time of referral.
Presentation Of The Case:
We report a 44-year-old man with primary malignant pericardial mesothelioma. He was referred to our hospital for the diagnosis and treatment of a massive pericardial effusion and huge tumor. Pericardiocentesis was performed, but we could not obtain definitive diagnosis, and the cardiac tamponade continued along with the signs/symptoms. He required surgical intervention for the diagnosis and treatment. After surgery, his signs/symptoms improved. He received adjuvant therapy, although he died 7 months after surgery.
Discussion:
Primary malignant pericardial mesothelioma is a rare tumor. The most common signs and symptoms are related to constriction of the heart by the tumor and/or effusion. Even if the pericardial fluid specimen obtained by pericardiocentesis is negative for malignant cells, primary malignant pericardial mesothelioma should be included in the differential diagnosis. Because the malignancy is usually advanced at the time of diagnosis, it has been difficult to cure. Radiation and chemotherapy have been used in addition to surgery, but have been minimally effective.
Conclusion:
The outcome of our patient with pericardial malignant mesothelioma was dismal. The indications for surgical intervention should be carefully considered except for critical cases requiring alleviation of immediate life-threating conditions.
Insights
Primary malignant pericardial mesothelioma is a rare and lethal cancer. Early diagnosis is challenging, and even with treatment, outcomes remain poor, highlighting the need for careful consideration of surgical intervention.
Area of Science:
- Oncology
- Cardiology
- Pathology
Background:
- Primary malignant pericardial mesothelioma is an exceptionally rare and aggressive malignancy.
- Diagnosis is often delayed due to nonspecific symptoms and challenges in initial testing.
- The disease carries a poor prognosis, with advanced stage at presentation being common.
Observation:
- A case of a 44-year-old male with primary malignant pericardial mesothelioma is presented.
- Massive pericardial effusion and a large tumor necessitated surgical intervention.
- Despite initial improvement post-surgery, the patient succumbed to the disease within 7 months.
Findings:
- Pericardiocentesis may not yield a definitive diagnosis, necessitating further investigation.
- Malignant cells in pericardial fluid are not always present, complicating diagnosis.
- Surgical intervention can alleviate symptoms but has not proven curative.
Implications:
- Primary malignant pericardial mesothelioma requires a high index of suspicion, even with negative initial diagnostic tests.
- Current treatment modalities including surgery, chemotherapy, and radiation show limited efficacy.
- Careful consideration of surgical indications is crucial, balancing potential benefits against risks.
More Related Videos
09:16Isolation and Characterization of Cardiac Mesenchymal Stromal Cells from Endomyocardial Bioptic Samples of Arrhythmogenic Cardiomyopathy Patients
Published on: February 28, 2018
07:54Implantation and Monitoring by PET/CT of an Orthotopic Model of Human Pleural Mesothelioma in Athymic Mice
Published on: December 21, 2019
Related Concept Videos
Pericarditis II: Clinical Features and Diagnostic Tests
Pericarditis III: Medical Management
Pericarditis IV: Nursing Management
Pericarditis I: Introduction
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy I: Introduction and Classification