Case Report: Neuroendocrine Tumor With Cardiac Metastasis
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 a...
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Format: | Article |
Language: | English |
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Frontiers Media S.A.
2020-12-01
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Series: | Frontiers in Cardiovascular Medicine |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fcvm.2020.596921/full |
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author | Rachel E. Kinney Robert Decker Deborah Sundlof Muhammad A. Rizvi Kelly Schadler |
author_facet | Rachel E. Kinney Robert Decker Deborah Sundlof Muhammad A. Rizvi Kelly Schadler |
author_sort | Rachel E. Kinney |
collection | DOAJ |
description | 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. |
first_indexed | 2024-12-17T22:28:02Z |
format | Article |
id | doaj.art-f0f968e2fb6041719f37b3d6acd5068a |
institution | Directory Open Access Journal |
issn | 2297-055X |
language | English |
last_indexed | 2024-12-17T22:28:02Z |
publishDate | 2020-12-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Cardiovascular Medicine |
spelling | doaj.art-f0f968e2fb6041719f37b3d6acd5068a2022-12-21T21:30:18ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2020-12-01710.3389/fcvm.2020.596921596921Case Report: Neuroendocrine Tumor With Cardiac MetastasisRachel E. KinneyRobert DeckerDeborah SundlofMuhammad A. RizviKelly SchadlerNeuroendocrine 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.https://www.frontiersin.org/articles/10.3389/fcvm.2020.596921/fullneuroendocrine tumorintracardiac metastasesileal neuroendocrine tumorinfiltrative myocardial metastasis177Lu DOTATATE |
spellingShingle | Rachel E. Kinney Robert Decker Deborah Sundlof Muhammad A. Rizvi Kelly Schadler Case Report: Neuroendocrine Tumor With Cardiac Metastasis Frontiers in Cardiovascular Medicine neuroendocrine tumor intracardiac metastases ileal neuroendocrine tumor infiltrative myocardial metastasis 177Lu DOTATATE |
title | Case Report: Neuroendocrine Tumor With Cardiac Metastasis |
title_full | Case Report: Neuroendocrine Tumor With Cardiac Metastasis |
title_fullStr | Case Report: Neuroendocrine Tumor With Cardiac Metastasis |
title_full_unstemmed | Case Report: Neuroendocrine Tumor With Cardiac Metastasis |
title_short | Case Report: Neuroendocrine Tumor With Cardiac Metastasis |
title_sort | case report neuroendocrine tumor with cardiac metastasis |
topic | neuroendocrine tumor intracardiac metastases ileal neuroendocrine tumor infiltrative myocardial metastasis 177Lu DOTATATE |
url | https://www.frontiersin.org/articles/10.3389/fcvm.2020.596921/full |
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