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Primary neuroendocrine tumours of the heart: case report and literature review
  1. Ellery Altshuler1,
  2. Haneen Saker1 and
  3. Brian Ramnaraign1,2
  1. 1Internal Medicine, University of Florida College of Medicine, Gainesville, Florida, USA
  2. 2Hematology and Oncology, UF Health Shands Hospital, Gainesville, Florida, USA
  1. Correspondence to Dr Ellery Altshuler; ElleryAltshuler{at}gmail.com

Abstract

Neuroendocrine tumours occur most frequently in the gastrointestinal tract, lungs, and pancreas. Primary malignant cardiac tumours are uncommon and are usually sarcomas, lymphomas, or, infrequently, mesotheliomas. Primary cardiac neuroendocrine carcinomas are exceedingly rare; only nine have been reported in the literature to date. We report the tenth case of this disorder in a 44-year-old man with a well-differentiated low-grade primary cardiac neuroendocrine carcinoma treated with surgery who remains in remission more than a year later. Our case and review of the literature demonstrate that surgical treatment for well-differentiated primary cardiac neuroendocrine carcinomas can be effective.

  • cardiovascular medicine
  • cancer - see oncology
  • interventional cardiology
  • cancer intervention

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Footnotes

  • Twitter @RamnaraignMD

  • Contributors BR conceived the idea for the manuscript and is responsible for its final content. EA and HS assisted with research and were primarily responsible for writing the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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