Case Report: Neuroendocrine Tumor With Cardiac Metastasis
- PMID: 33425998
- PMCID: PMC7793920
- DOI: 10.3389/fcvm.2020.596921
Case Report: Neuroendocrine Tumor With Cardiac Metastasis
Abstract
Neuroendocrine tumors (NETs), also known as carcinoid tumors, are a heterogeneous group of neoplasms that arise from cells throughout the neuroendocrine system, most commonly arising from the gastrointestinal (GI) tract, lungs, and bronchi. Myocardial carcinoid metastasis is rare with an incidence among metastatic carcinoid patients of 4%. They are generally asymptomatic and detected incidentally. Infiltrative myocardial metastasis secondary to carcinoid tumor is exceedingly rare with only single-digit cases reported in the literature. We report the case of a 65-years-old female with a newly diagnosed ileal neuroendocrine tumor as well as heart failure due to infiltrative myocardial metastasis.
Keywords: 177Lu DOTATATE; ileal neuroendocrine tumor; infiltrative myocardial metastasis; intracardiac metastases; neuroendocrine tumor.
Copyright © 2020 Kinney, Decker, Sundlof, Rizvi and Schadler.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
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- National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology, Neuroendocrine and Adrenal Tumors. Version 1.2019 (2019). - PubMed