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Updated: May 21, 2026
07:55
Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Primary liposarcoma of the heart
1Department of Pathology, Innsbruck Medical University, Innsbruck, Austria. christina.m.steger@i-med.ac.at
BMJ Case Reports
|June 15, 2012
Summary
A large pericardial liposarcoma was successfully resected in a 64-year-old man. The patient remains recurrence-free two years post-surgery, highlighting successful treatment for this rare cardiac tumor.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Pericardial tumors are rare, often presenting with nonspecific symptoms.
- Early diagnosis and complete resection are crucial for favorable outcomes.
Observation:
- A 64-year-old male presented with dyspnea and dizziness due to a large pericardial mass.
- Chest CT revealed a lobulated mass in the pericardial sac, compressing vital structures.
Findings:
- Histopathological analysis confirmed a well-differentiated lipoma-like and focal sclerosing liposarcoma.
- The tumor predominantly consisted of adipocytes with specific cytological and structural features.
Implications:
- Complete surgical resection can lead to long-term survival in patients with pericardial liposarcoma.
- This case underscores the importance of thorough histopathological examination for accurate tumor classification and management.
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