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Cardiac lymphoma involving the right heart

Dror B Leviner

Department of Cardiothoracic Surgery, Rabin Medical Center, Beilinson Campus, Israel

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Eitan Snir

Department of Cardiothoracic Surgery, Rabin Medical Center, Beilinson Campus, Israel

Dan Aravot

Department of Cardiothoracic Surgery, Rabin Medical Center, Beilinson Campus, Israel

Milton Saute

Department of Cardiothoracic Surgery, Rabin Medical Center, Beilinson Campus, Israel

DOI: 10.15761/SCRR.1000137

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Key words

Cardiac Tumors, Echocardiography

Case study

A 63-year-old woman with a medical history of smoking and epilepsy was hospitalized after a two-week period of shortness of breath. Her physical examination was notable for tachycardia and distant heart sounds. She underwent a transesophageal echocardiogram which showed a large mass engulfing the right ventricle and atrium, infiltrating the free wall of the ventricle into the tricuspid valve and compressing the superior vena cave (Figure 1). A chest CT revealed a large mass infiltrating the right ventricle and atrium and intruding the SVC (Figure 2). She was hemodynamically stable. A multidisciplinary team decided that a biopsy was necessary. The post-operative course was uneventful. The biopsy specimen showed a diffuse large B-cell lymphoma (Figure 3). Chemotherapy was immediately started.

Figure 1. Transesophageal echocardiogram - Parasternal long axis view with the mass attached to the RV and RA

Figure 2. ECG gated contrast enhanced CT - coronal reconstruction demonstrating the mass engulfing the RVOT and the aortic root

Figure 3. H&E staining (X40) showing diffuse sheets of lymphoma cells

Primary cardiac lymphomas comprise only 1% of all primary cardiac tumors, which are rarer than metastatic tumors of the heart [1]. B-cell lymphoma is the most common type, typically involving the right cardiac chambers. Presentation usually includes signs of obstruction or emboli. Treatment is based on chemotherapy and radiotherapy, with better prognosis than that of other cardiac malignancies [2].

References

  1. Reynen K (1996) Frequency of primary tumors of the heart. Am J Cardiol 77: 107. [Crossref]
  2. Nascimento AF, Winters GL, Pinkus GS (2007) Primary cardiac lymphoma: clinical, histologic, immunophenotypic, and genotypic features of 5 cases of a rare disorder. Am J Surg Pathol 31: 1344-1350. [Crossref]

Editorial Information

Editor-in-Chief

Article Type

Case report

Publication History

Received: June 01, 2019
Accepted: June 10, 2019
Published: June 13, 2019

Copyright

©2019 Saute M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Saute M (2019) Cardiac lymphoma involving the right heart. Surg Case Rep Rev, 3. DOI: 10.15761/SCRR.1000137

Corresponding author

Milton Saute

Department of Cardiothoracic Surgery, Rabin Medical Center, Beilinson Campus, Petach Tiqva 49100, Israel

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Figure 1. Transesophageal echocardiogram - Parasternal long axis view with the mass attached to the RV and RA

Figure 2. ECG gated contrast enhanced CT - coronal reconstruction demonstrating the mass engulfing the RVOT and the aortic root

Figure 3. H&E staining (X40) showing diffuse sheets of lymphoma cells