| Literature DB >> 33443717 |
Kira Oleinikov1,2, Amit Korach2,3, David Planer2,4, Dan Gilon2,4, Simona Grozinsky-Glasberg5,6.
Abstract
Carcinoid heart disease (CHD) is a paraneoplastic cardiac manifestation occurring in patients with carcinoid syndrome (CS) and advanced neuroendocrine malignancy. In about 20-40% of patients with CS, chronic exposure to tumor-released circulating vasoactive peptides typically results in right-sided valvular fibrosis leading to valve dysfunction and right heart failure. CHD remains a significant cause of morbidity and mortality. The management of patients with CHD is complex, as both the systemic malignant disease and the heart involvement have to be addressed. Early diagnosis and timely surgical intervention in selected patients are of utmost importance and offer a survival benefit. In patients with advanced carcinoid heart disease, valve replacement surgery is the most effective option to alleviate cardiac symptoms and contribute to survival outcomes. A collaboration of a multidisciplinary team in centers with experience is required to provide optimal patient management. Here, we review the current literature regarding CHD presentation, pathophysiology, diagnostic tools, and available treatment strategies.Entities:
Keywords: 5-HT; 5-hydroxytryptamine; B-type natriuretic peptide; Carcinoid heart disease; Carcinoid syndrome; Echocardiography; Heart valve disease; NT-proBNP; Neuroendocrine tumor
Mesh:
Year: 2021 PMID: 33443717 DOI: 10.1007/s11154-020-09624-y
Source DB: PubMed Journal: Rev Endocr Metab Disord ISSN: 1389-9155 Impact factor: 9.306