Case 57

Published on 13/02/2015 by admin

Filed under Cardiovascular

Last modified 22/04/2025

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CASE 57

image

ANSWERS

CASE 57

Pericardial Lymphoma

1A, B, C, and D

2A

3A

4D

Reference

Yared K, Baggish AL, Picard MH, et al. Multimodality imaging of pericardial diseases. JACC Cardiovasc Imaging. 2010;3(6):650–660.

Cross-Reference

Cardiac Imaging: The REQUISITES, ed 3, pp 102–104.

Comment

Radiographic Features

Most pericardial tumors are secondary to direct extension or hematogenous spread from lung or breast carcinoma, lymphoma, and melanoma. Findings suggestive of pericardial malignancy include enhancing pericardial nodules or masses and hemopericardium. Primary pericardial tumors are rare; mesothelioma is the most common. Other primary pericardial tumors include lymphoma and teratoma.

Primary Cardiac Lymphoma

Primary pericardial lymphoma is associated with acquired immunodeficiency syndrome (AIDS) and is generally a non-Hodgkin lymphoma. By definition, the lymphoma is localized to the heart or pericardium at diagnosis without evidence of systemic disease. Presenting symptoms include rapidly progressive heart failure, arrhythmia, cardiac tamponade, superior vena cava syndrome, and chest pain. Pleural effusion, including hemorrhagic effusion, occurs frequently. The prognosis of primary cardiac lymphoma is poor with many patients being diagnosed at autopsy. Treatment includes chemotherapy and tumor debulking for palliative control of symptoms.

Imaging

CT is frequently performed for diagnosis, but MRI is especially useful to define the extent of involvement. Lymphoma is typically infiltrative and follows the pericardial contour (Figure). Both CT and MRI show heterogeneous enhancement following the administration of intravenous contrast. Cross-sectional imaging plays an important role in assessing disease response to therapy.