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Isolation of Atrial Myocytes from Adult Mice
Published on: July 25, 2019
Primary extramedullary plasmacytoma in the atria of the heart
X Wan1, S Tarantolo, D F Orton
1Department of Pathology and Microbiology, University of Nebraska Medical Center, 983332 Nebraska Medical Center, 68198-3332, Omaha, NE, USA.
Insights
A rare primary extramedullary plasmacytoma of the heart caused severe cardiovascular issues. Diagnosis involved biopsy and immunohistochemistry, highlighting kappa light chain expression.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Primary extramedullary plasmacytoma is a rare plasma cell neoplasm.
- Cardiac tumors can present with significant cardiovascular compromise.
Observation:
- A large, space-occupying tumor in the atrial wall led to impaired cardiovascular function.
- Significant pericardial effusion was associated with the cardiac tumor.
Findings:
- Diagnosis was confirmed via intravenous biopsy and immunohistochemistry.
- Tumor cells expressed CD45 and kappa light chains, with negative B-cell and T-cell markers.
- Serum immunofixation electrophoresis revealed elevated kappa light chains.
Implications:
- Consider plasmacytoma in cardiac tumors when routine lymphoid and soft tissue markers are negative.
- Immunohistochemistry, including kappa light chain detection, is crucial for diagnosing rare cardiac neoplasms.
- This case expands the understanding of extramedullary plasmacytoma localization and presentation.
Abstract:
A rare case of primary extramedullary plasmacytoma of the heart is described. The large space-occupying tumor in the atrial wall and its associated significant pericardial effusion caused marked impairment of cardiovascular function. The diagnosis was made via intravenous biopsy. Immunohistochemistry demonstrated CD45 and kappa light chain expression. Other B-cell- and T-cell-specific lymphoid markers were negative. Elevated kappa light chain was detected in serum by immunofixation electrophoresis. The differential diagnosis of plasmacytoma should be considered in cardiac tumors when routine screening is negative with lymphoid (CD20, CD3) and soft tissue immunohistochemical markers.
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