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Diffuse infiltrative primary cardiac lymphoma with delayed extracardiac involvement.
Yong Jeoung1, Se Ryeon Lee1, Ho Kim1
1Department of Internal Medicine, Korea University Medical Center, Seoul, Korea.
Chonnam Medical Journal
|May 24, 2014
Summary
Primary cardiac lymphoma (PCL), a rare heart cancer, poses diagnostic challenges. This case highlights a delayed diagnosis of diffuse large B cell lymphoma (DLBCL) involving the heart, emphasizing the need for thorough investigation.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Primary cardiac lymphoma (PCL) is exceptionally rare, often fatal, and difficult to diagnose due to its location and infiltrative nature.
- The prognosis for PCL is generally poor, compounded by challenges in early and accurate diagnosis.
Observation:
- A 48-year-old male presented with pericardial effusion and diffuse cardiac wall thickening, initially suspected as infiltrative heart disease.
- Initial biopsies were inconclusive, delaying definitive diagnosis for 20 months.
Findings:
- The patient was ultimately diagnosed with primary cardiac diffuse large B cell lymphoma (DLBCL) via a cervical lymph node biopsy.
- Chemotherapy led to significant improvement in DLBCL lesions, including cardiac wall thickening.
Implications:
- This case underscores the diagnostic complexities of infiltrative primary cardiac lymphoma (PCL).
- The findings suggest PCL can present with delayed extracardiac involvement, necessitating comprehensive evaluation.
- Successful treatment with chemotherapy indicates its potential efficacy in managing cardiac lymphoma.
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