Results 261 to 270 of about 2,893,372 (329)
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Carcinoid Tumors

Current Problems in Surgery, 2006
Carcinoid tumors can present a difficult diagnostic and therapeutic dilemma. Despite their reputation as indolent tumors, they frequently metastasize and can cause significant symptomatology. The only curative therapy remains surgical resection. The prognosis and treatment of carcinoids vary based on location and histology, and therapy must be tailored
Chandrajit P, Raut   +4 more
semanticscholar   +5 more sources

Management of Carcinoid Tumors

open access: yesThe Annals of Thoracic Surgery, 2010
Primary bronchopulmonary carcinoids comprise a significant proportion of carcinoid tumors. The clinical presentation allows prediction of the diagnosis and cell type and directs evaluation and treatment. Young age, central tumor, and no nodal enlargement are highly suggestive of typical carcinoid. These patients require no further diagnostic or staging
F. Detterbeck
openaire   +4 more sources

Contributions of Adenocarcinoma and Carcinoid Tumors to Early-Onset Colorectal Cancer Incidence Rates in the United States

Annals of Internal Medicine, 2020
BACKGROUND Early-onset colorectal cancer (EOCRC) incidence rates (IRs) are rising, according to previous cancer registry analyses. However, analysis of histologic subtypes, including adenocarcinoma (the focus of CRC screening and diagnostic testing) and ...
Eric M. Montminy   +8 more
semanticscholar   +1 more source

Carcinoid tumors

Current Treatment Options in Oncology, 2002
Carcinoids are rare endocrine tumors that can develop in several organs in the body. Clinically, patients can have a wide spectrum of signs and symptoms that range from incidental findings of a polyp during endoscopy to the carcinoid syndrome characterized by severe flushing, diarrhea, abdominal cramping, and life-threatening right-sided heart failure.
Alan P.B. Dackiw, Robin P. Boushey
openaire   +3 more sources

One hundred years after "carcinoid": epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States.

Journal of Clinical Oncology, 2008
PURPOSE Neuroendocrine tumors (NETs) are considered rare tumors and can produce a variety of hormones. In this study, we examined the epidemiology of and prognostic factors for NETs, because a thorough examination of neither had previously been performed.
James C. Yao   +10 more
semanticscholar   +1 more source

CARCINOID TUMORS AND THE CARCINOID SYNDROME

Journal of the American Geriatrics Society, 1969
AbstractData are presented on 10 cases of carcinoid tumor; 8 of the tumors were in the gastrointestinal tract and 2 in the lung. Two cases were associated with carcinoid syndrome (flushing attacks, diarrhea, bronchospasm); in one of these with marked symptoms, the 24‐hour excretion of 5 hydroxy indole acetic acid reached 107 mg.On the basis of these ...
F.A.G.S. Majid-Uddin Kazi M.D.   +1 more
openaire   +3 more sources

Carcinoid Tumors

Archives of Surgery, 1984
A retrospective study of 86 patients with carcinoid tumors was undertaken covering an 18-year period. The most common sites of tumor were the jejunoileum (28 cases), appendix (22), and rectum (16). These were followed by the bronchus, duodenum, colon, and stomach. Three tumors had such wide-spread metastasis that their primary sites of origin could not
L, Dawes, W J, Schulte, R E, Condon
openaire   +2 more sources

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