Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2020 Jan;9(1):394-399.
doi: 10.21037/tcr.2019.11.42.

Rarely seen primary cardiac natural killer/T cell lymphoma: a case report

Affiliations
Case Reports

Rarely seen primary cardiac natural killer/T cell lymphoma: a case report

Xin Yang et al. Transl Cancer Res. 2020 Jan.

Abstract

Primary cardiac lymphoma is an extremely rare malignancy, which is typically of a non-Hodgkin's type. Clinical manifestations including dyspnea, arrhythmia, chest pain and so on, may vary according to heart site involved and the right atrium is most frequently involved. Histologically, the majority of primary cardiac lymphomas are B-cell origin, especially diffuse large B-cell lymphoma. Here we report a case of primary cardiac nature killer/T cell lymphoma arising in a 40-year-old woman, who presented with paroxysmal chest congestion, nausea and ventricular tachycardia, and diagnosed by open chest surgery and whole body PET/CT scan, then treated with three cycles of chemotherapy, but finally died of multiple organ failure. The optimal treatment strategies to primary cardiac lymphoma have not been fully defined due to its rarity, which still needs to gather more cases and conduct further researches.

Keywords: Epstein-Barr virus (EBV); NK/T cell; Primary cardiac lymphoma; case report.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr.2019.11.42). The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Positron emission tomography–computed tomography (PET/CT) scan. Only a mass of accelerated glycolytic metabolism (SUV 7.1) at right atrioventricular groove was found (A), and the representative images of abdominal cavity (B), pelvic cavity (C), and nasal cavity (D) are shown as well.
Figure 2
Figure 2
Immunohistochemistry of extra-nodal NK/T-cell lymphoma, nasal type. Hematoxylin and eosin stained sections of the mass reveals a dense infiltrate of primarily small lymphocytes with irregular nuclear contours (A) and immunohistochemistry shows the neoplastic cell co-express CD3ε (B) and CD56 (C). Almost all of the neoplastic cells are Ki67 positive (D), and neoplastic cells showed EBER positive (E), but CD20 negative (F). Magnification: ×400.
Figure 3
Figure 3
Timeline of interventions and outcomes. MTX, methotrexate; DEX, dexamethasone; MOF, multiple organ failure.

References

    1. McAllister HA, Fenoglio JJ. Tumors of the cardiovascular system. In: Atlas of Tumor Pathology. 2nd Series. Fascicle15. Washington, DC: Armed Forces Institute of Pathology; 1978:99-100.
    1. Burke A, Virmani R. Tumors of the heart and great vessels. In: Atlas of Tumor Pathology. 3rd Series. Fascicle 16. Washington, DC: Armed Forces Institute of Pathology; 1996:171-9.
    1. Gowda RM, Khan IA. Clinical Perspectives of Primary Cardiac Lymphoma. Angiology 2003;54:599-604. 10.1177/000331970305400510 - DOI - PubMed
    1. Riley DS, Barber MS, Kienle GS, et al. CARE 2013 Explanations and Elaborations: Reporting Guidelines for Case Reports. J Clin Epidemiol 2017;89:218-35. 10.1016/j.jclinepi.2017.04.026 - DOI - PubMed
    1. Petrich A, Cho SI, Billett H. Primary cardiac lymphoma: an analysis of presentation, treatment, and outcome patterns. Cancer 2011;117:581-9. 10.1002/cncr.25444 - DOI - PubMed

Publication types