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Cytologically malignant lymphoid pericardial effusion with benign clinical outcome
Micha Maeder1, Peter Spieler, Reto Krapf
1Department of Internal Medicine, Cantonal Hospital of St. Gallen, Switzerland. micha.maeder@kssg.ch
Insights
DNA aneuploidy in pericardial fluid, initially suggestive of lymphoma, was found to be non-specific. Long-term survival in two patients indicates viral pericarditis, not primary cardiac or effusion lymphoma.
Area of Science:
- Oncology
- Pathology
- Cytometry
Background:
- Primary cardiac lymphoma (PCL) and primary effusion lymphoma (PEL) are rare non-Hodgkin's lymphomas (NHL) presenting as isolated malignant pericardial effusion.
- Diagnosis often involves cytological methods and DNA-image cytometry (ICM-DNA), with DNA-aneuploidy considered highly specific for malignancy.
Observation:
- Two patients with cardiac tamponade underwent pericardiocentesis for large pericardial effusions.
- Pericardial fluid analysis revealed atypical lymphoid cells and significant DNA-aneuploidy via ICM-DNA.
- Staging examinations did not reveal other tumor manifestations.
Findings:
- Despite highly atypical cytomorphology and DNA-aneuploidy, both patients achieved long-term cancer-free survival without systemic chemotherapy.
- This suggests pronounced reactive lymphocytic changes, likely due to viral pericarditis, rather than PCL or PEL.
Implications:
- DNA-aneuploidy in pericardial fluid may not be absolutely specific for detecting malignant lymphoid cells.
- Rethinking diagnostic criteria for pericardial effusions with atypical cytology and aneuploidy is warranted.
Background:
Isolated malignant pericardial effusion is a manifestation of primary cardiac lymphoma (PCL) and primary effusion lymphoma (PEL), rare types of non-Hodgkin's lymphoma (NHL). The diagnosis is based on different cytological methods and analyses including DNA-image cytometry (ICM-DNA). DNA-aneuploidy has been reported to be highly specific for malignancy.
Case Descriptions And Results:
A 75-year-old man and a 66-year-old woman underwent urgent pericardiocentesis for cardiac tamponade due to large pericardial effusion. In both patients pericardial fluid analysis showed highly atypical blastic lymphoid cells expressing CD45 (both patients) and CD20 (assessed only in one patient), and ICM-DNA revealed significant DNA-aneuploidy (2c deviation index 9.22 and 10.73 respectively, 75% and 60% respectively of the target nuclei in aneuploid areas). Extensive staging examinations did not identify any other tumour manifestation. Although in neither of the two patients systemic chemotherapy was administered, both were free of cancer after a follow-up of ten and nine years respectively.
Conclusions:
Despite the highly atypical cytomorphology including unequivocal DNA aneuploidy, long-term survival in both patients strongly suggests that pronounced reactive lymphocytic changes are probably due to viral pericarditis rather than PCL or PEL as underlying conditions. It seems that DNA-aneuploidy may be not absolutely specific for the detection of malignant lymphoid cells in pericardial fluid.
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