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Background: Carcinoid heart disease is a rare disease which develops in patients with functional neuroendocrine tumors in an advanced tumor state. Patients diagnosed with carcinoid heart disease have a poor longtime prognosis with respect to morbidity and mortality and long-term data on patient outcomes are lacking.
Methods And Results: In this retrospective study, we analyzed outcomes of 23 patients with carcinoid heart disease enrolled into the SwissNet database. We observed that early diagnosis with echocardiographic surveillance of carcinoid heart disease during the course of the neuroendocrine tumor disease was beneficial to overall survival of patients.
Conclusion: Through nationwide patient enrollment, the SwissNet registry is a powerful data tool to identify, follow-up and evaluate long-term patient outcomes in patients with rare neuroendocrine tumor driven pathologies including carcinoid heart syndrome with observational methods enabling better therapy optimization to improve patient`s long-term perspectives and survival. In line with the current ESMO recommendations, our data proposes that heart echocardiography should be included as part of the general physical assessment in patients with newly diagnosed NET.
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http://dx.doi.org/10.1186/s12885-023-10739-z | DOI Listing |
Cardiooncology
September 2025
Hospital Distrital de Santarém, Santarém, Portugal.
Background: Carcinoid Heart Disease (CHD) primarily affects the right heart valves, while left heart involvement is rare and often associated with a patent foramen ovale (PFO). Early identification of a PFO in CHD can be critical to patient outcomes. A 61-year-old woman with metastatic neuroendocrine tumor presented with worsening breathlessness and hypoxemia.
View Article and Find Full Text PDFSci Rep
August 2025
Paris Cité University and Sorbonne Paris Nord University, INSERM, LVTS, 75018, Paris, France.
Carcinoid heart disease, a severe complication of neuroendocrine tumors, affects up to 50% of patients and is challenging to treat due to a limited understanding of its mechanisms. The disease is characterized by structural remodeling and thickening of the right heart valves, associated with elevated levels of serotonin (5-HT) released from tumor cells that have spread to the liver. Existing animal models have limitations as they either use mice with compromised immune systems or employ methods that don't consistently evaluate valve changes.
View Article and Find Full Text PDFJ Community Hosp Intern Med Perspect
May 2025
Department of Hematology and Oncology, MedStar Health, Baltimore, USA.
Carcinoid tumors are rare, slow-growing neoplasms of neuroendocrine origin commonly affecting the gastrointestinal or respiratory system. They metastasize to lymph nodes and the liver based on their lymphatic and venous drainage of their tissue of origin. Metastasis to the heart is exceedingly rare accounting for <2 % of cases.
View Article and Find Full Text PDFMayo Clin Proc
August 2025
Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MN. Electronic address:
Objective: To evaluate the association of preoperative cardiac status and tumor characteristics with long-term survival after valve surgery for carcinoid heart disease (CHD).
Methods: A retrospective review was conducted of patients surgically treated for CHD at our institution between 2000 and 2023.
Results: A total of 168 patients (median age, 63.
Cureus
June 2025
Cardiovascular Medicine, Pueblo Cardiology Associates, Pueblo, USA.
Carcinoid heart disease (CHD) is a severe complication of metastatic neuroendocrine tumors (NETs), leading to fibrotic degeneration of right-sided heart valves. A 38-year-old male presented with progressive dyspnea, fatigue, abdominal bloating, diarrhea, and facial flushing. Imaging revealed hepatic metastases and mesenteric lymphadenopathy, and biochemical markers confirmed a NET of likely gastrointestinal origin.
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