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Clinical manifestation of neuroendocrine tumor – carcinoid heart disease
Medical alphabet, 2023Carcinoid heart disease (CHD) is a rare manifestation of the carcinoid syndrome, but eventually occurs in most patients and is a major cause of cardiovascular mortality.
F. R. Akildzhonov +6 more
semanticscholar +1 more source
Clinical Nuclear Medicine
Carcinoid heart disease (Hedinger syndrome) is a long-term consequence in hormone-active neuroendocrine tumors with hepatic metastases and carcinoid syndrome.
C. Laschinsky +4 more
semanticscholar +1 more source
Carcinoid heart disease (Hedinger syndrome) is a long-term consequence in hormone-active neuroendocrine tumors with hepatic metastases and carcinoid syndrome.
C. Laschinsky +4 more
semanticscholar +1 more source
Two- and Three-dimensional Imaging in Carcinoid Heart Disease
Journal of The Indian Academy of Echocardiography & Cardiovascular ImagingA 70-year-old male presented with a history of pedal edema, abdominal distension, and dyspnea on exertion New York Heart Association Class III for cardiology evaluation.
Abhiman Balakrishna Shetty +2 more
semanticscholar +1 more source
Circulation, 2023
Carcinoid tumors are neuroendocrine neoplasms that secrete vasoactive substances, primarily serotonin, and have an incidence of approximately 2 in 100,000 people.
Jordan Troy +4 more
semanticscholar +1 more source
Carcinoid tumors are neuroendocrine neoplasms that secrete vasoactive substances, primarily serotonin, and have an incidence of approximately 2 in 100,000 people.
Jordan Troy +4 more
semanticscholar +1 more source
Circulation, 2023
Background: Patients with carcinoid heart disease are prone to the development of mild to severe tricuspid regurgitation with or without accompanying tricuspid stenosis.
Suma Pusapati +2 more
semanticscholar +1 more source
Background: Patients with carcinoid heart disease are prone to the development of mild to severe tricuspid regurgitation with or without accompanying tricuspid stenosis.
Suma Pusapati +2 more
semanticscholar +1 more source
Endocrinology and Metabolism Clinics of North America, 2018
Carcinoid heart disease remains a major cause of morbidity and mortality among patients with carcinoid syndrome and metastatic neuroendocrine tumors. Screening of all patients with N-terminal pro-B-type natriuretic peptide and transthoracic echocardiography is critical for early detection, as early symptoms and signs have low sensitivity for the ...
Martyn Caplin +2 more
openaire +3 more sources
Carcinoid heart disease remains a major cause of morbidity and mortality among patients with carcinoid syndrome and metastatic neuroendocrine tumors. Screening of all patients with N-terminal pro-B-type natriuretic peptide and transthoracic echocardiography is critical for early detection, as early symptoms and signs have low sensitivity for the ...
Martyn Caplin +2 more
openaire +3 more sources
Carcinoid Heart Disease: A Rare Complication of Metastatic Neuroendocrine Tumor
Pakistan Journal of Medical & Health Sciences, 2023Background: Carcinoid heart disease (CHD) is a rare but severe complication of metastatic neuroendocrine tumors (NETs), primarily affecting the right-sided heart valves due to prolonged exposure to vasoactive substances such as serotonin. Objective: This
A. Qasim +5 more
semanticscholar +1 more source
Carcinoid Heart Disease – A 2022 Retrospective
Romanian Journal of Military Medicine, 2023" We aim to introduce a 2022 update on CHD (carcinoid heart disease) considering a multidisciplinary perspective. This is a narrative mini-review. We searched English, full-length papers (PubMed).
C. Nistor +3 more
semanticscholar +1 more source
Palliation of Carcinoid Heart Disease
Archives of Surgery, 1987The clinical manifestations of the carcinoid syndrome have been known for 35 years. Median survival in patients with carcinoid syndrome, although dependent on several factors, including the extent of liver metastases, is in the range of four years. In this setting, a frequent cause of death is right-sided cardiac dysfunction. When this occurs, the only
John E. Codd, Joseph Drozda, Merjavy Jp
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Circulation, 1996
A53-year-old Indian man developed watery diarrhea. He was treated for inflammatory bowel disease without improvement. Three months before admission, he developed lower extremity edema, which progressed to include massive scrotal edema as well as dyspnea on exertion, orthopnea, and paroxysmal nocturnal dyspnea.
Daniel J. Krauss +3 more
openaire +2 more sources
A53-year-old Indian man developed watery diarrhea. He was treated for inflammatory bowel disease without improvement. Three months before admission, he developed lower extremity edema, which progressed to include massive scrotal edema as well as dyspnea on exertion, orthopnea, and paroxysmal nocturnal dyspnea.
Daniel J. Krauss +3 more
openaire +2 more sources