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[Primary lymphoma of the heart: difficulties in diagnosis and treatment]
Insights
Primary cardiac lymphoma, a rare B-cell non-Hodgkin's lymphoma, presents diagnostic challenges. This case highlights a patient with pre-existing cardiac conditions who developed lymphoma, ultimately succumbing to complications despite chemotherapy.
Area of Science:
- Cardiology
- Oncology
- Pathology
Background:
- Primary cardiac lymphoma is a rare malignancy, accounting for 1.3-2.0% of primary heart tumors.
- The case involves a 43-year-old male with a history of ventricular tachycardia, AB-block, hypertrophic cardiomyopathy, and pericardial effusion.
Observation:
- The patient experienced worsening dyspnea, right ventricular hypertrophy, and elevated cardiac pressures.
- Imaging revealed a massive tumor in the heart and mediastinum, initially misdiagnosed as sarcoma.
- Biopsies confirmed diffuse large B-cell lymphoma involving the liver and lymph nodes.
Findings:
- The patient underwent pulmonary artery valve balloon angioplasty prior to lymphoma diagnosis.
- Despite effective chemotherapy (CHOP), the patient developed mesenterial thrombosis and died.
Implications:
- This case underscores the diagnostic complexities of primary cardiac lymphoma, especially in patients with pre-existing cardiac conditions.
- It highlights the critical need for accurate and timely diagnosis and the challenges in managing treatment strategies for this rare disease.
Abstract:
Primary lymphoma of the heart (non-Hodgkin's lymphoma primarily of B-cells affecting first the heart and pericardium) is a rare disease which accounts for 1.3-2.0% of all primary tumors of the heart. A case is reported of a 43-year-old male patient with a cardioverter-defibrillator implanted at the age of 38 years for management of ventricular tachycardia paroxysms and AB-block of the second-third degree. The patient also had hypertrophic cardiomyopathy, moderate pressure gradient on the pulmonary artery valve and pericardial effusion. Later he had two cardiac tamponades (serous punctuate). From the age of 42 years breathlessness, right ventricular wall thickness, right heart pressure and pulmonary artery pressure aggravated. The patient has undergone ballon plastic surgery of the pulmonary artery valve. At the age of 43 computed tomography detected massive tumor of the heart and mediastinum first diagnosed as sarcoma but later specified as lymphoma. Endobronchial biopsy specimens contained the tissue of diffuse large B-cell lymphoma, the liver and lymph nodes were also involved. After the first course of effective polychemotherapy (CHOP) the patient died of mesenterial thrombosis. Diagnostic difficulties and problems of treatment policy are discussed.
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