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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Main Authors: Rachel E. Kinney, Robert Decker, Deborah Sundlof, Muhammad A. Rizvi, Kelly Schadler
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
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.
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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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