[Primary pericardial malignant mesothelioma with incomplete endocardial cushion defect; report of a case]
Takashi Okamoto1, H Doi, J Yasuike
1Department of Cardiovascular Surgery, Cardio-vascular Center Hokkaido Ohno Hospital, Sapporo, Japan.
Abstract:
Primary pericardial malignant mesothelioma is rare tumor and its prognosis is quite poor due to its late presentation and difficulty of complete resection. We describe a rare case of primary pericardial malignant mesothelioma in a 46-year-old female with incomplete endocardial cushion defect (ECD). Incidentally, we found 2 masses in the pericardial spaces after pericardiectomy. We have successfully removed these 2 masses en bloc and performed a total repair of incomplete ECD. Pathologically, these masses were a primary pericardial malignant mesothelioma. This patient is doing well 4 months after surgery without any evidence of recurrence despite reported poor prognosis of "primary pericardial malignant mesothelioma".
Insights
A rare primary pericardial malignant mesothelioma case in a woman with a heart defect was successfully treated. Surgical removal of the tumor and heart defect repair led to a positive outcome with no recurrence.
Area of Science:
- Cardiovascular Surgery
- Thoracic Oncology
- Pathology
Background:
- Primary pericardial malignant mesothelioma is a rare and aggressive tumor with a poor prognosis.
- Late presentation and challenges in complete surgical resection contribute to its poor outcomes.
- Co-occurrence with congenital heart defects like incomplete endocardial cushion defect (ECD) is exceptionally rare.
Observation:
- A 46-year-old female presented with symptoms necessitating pericardiectomy.
- During surgery for an incomplete endocardial cushion defect (ECD), two masses were incidentally discovered in the pericardial space.
- The masses were successfully removed en bloc along with the total repair of the incomplete ECD.
Findings:
- Pathological examination confirmed the masses to be primary pericardial malignant mesothelioma.
- The patient underwent successful surgical management involving en bloc resection of the mesothelioma and complete repair of the incomplete ECD.
- Post-operative follow-up at 4 months showed no evidence of tumor recurrence.
Implications:
- This case highlights the possibility of successful surgical management for primary pericardial malignant mesothelioma, even in the presence of congenital heart defects.
- Aggressive surgical resection, when feasible, may offer a favorable outcome despite the tumor's generally poor prognosis.
- Further research into multimodal treatment strategies for this rare malignancy is warranted.
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