Results 11 to 20 of about 115,541 (278)

Carcinoid tumors outside the abdomen [PDF]

open access: yesCancer Medicine, 2023
Neuroendocrine tumors (NETs) are epithelial malignancies that can arise from multiple tissues. Gastrointestinal (GI) NETs are the most common; in this review of extra‐abdominal carcinoid tumors, we focus our discussion on bronchial and thymic carcinoid ...
Kenna Koehler, Wade T. Iams
doaj   +2 more sources

Carcinoid tumors [PDF]

open access: yesOrvosi Hetilap, 2010
A szerzők a carcinoid tumorokkal kapcsolatos legfontosabb klinikai gyakorlati ismeretekről adnak áttekintést. A carcinoid daganatok neuroendokrin sejtekből származó, többségében lassan növekvő ritka tumorok, azonban gyorsan metasztatizáló, agresszív formában is jelentkezhetnek. Epidemiológiai adatok szerint gyakoriságuk nő, amit részben a diagnosztikus
István, Pregun   +3 more
openaire   +5 more sources

Clinical, pathological characteristics, and therapeutic outcomes of primary ovarian carcinoid tumors: a case series of 15 cases [PDF]

open access: yesWorld Journal of Surgical Oncology
Background The exact characteristics of primary ovarian carcinoid tumors remain largely unknown because of the rarity of the cases. This study aimed to investigate the clinical features, pathological characteristics, and therapeutic outcomes of patients ...
Xinyue Dai, Suidan Chen, Simeng Yang
doaj   +2 more sources

Carcinoid tumors of the thymus [PDF]

open access: bronzeCancer, 1976
Three patients with carcinoid tumors of the anterior mediastinum are described. Study of these patients and an analysis of previously reported cases indicates that the thymus is the primary site of these tumors, which are probably related to the presence of Kulchitsky cells in normal thymus.
William R. Salyer   +2 more
openalex   +4 more sources

Surgical management of both stage III and stage IV pulmonary carcinoid tumors confers survival benefitCentral MessagePerspective [PDF]

open access: yesJTCVS Open
Objective: Pulmonary carcinoid tumors are an uncommon entity, with an incidence of 1.35 cases per 100,000 individuals. Although decisions about surgical resection are commonly made similarly to those for non–small cell lung cancer, data surrounding the ...
J. Asher Jenkins, MD   +12 more
doaj   +2 more sources

Heterogeneous tumor‐immune microenvironments between primary and metastatic carcinoid tumors differentially respond to anti‐PD‐L1 antibody therapy [PDF]

open access: yesThoracic Cancer, 2021
A pulmonary carcinoid tumor is a rare tumor that lacks a validated therapeutic approach for unresectable disease. Understanding the intersite tumor‐immune heterogeneity is essential to harness the immune system for cancer therapy.
Shinya Sakata   +9 more
doaj   +2 more sources

Carcinoid Tumors [PDF]

open access: yesThe Oncologist, 2008
Abstract Carcinoid tumors are rare, slow-growing neuroendocrine tumors arising from the enterochromaffin cells disseminated throughout the gastrointestinal and bronchopulmonary systems. Though they have been traditionally classified based on embryologic site of origin, morphologic pattern, and silver affinity, newer classification ...
Scott N, Pinchot   +3 more
openaire   +3 more sources

Incidentally Found Rectal Carcinoid Tumor in a 46-Year-Old Female: The Potential for Complications and the Importance of Screening Guidelines

open access: yesInternational Journal of Medical Students, 2023
BACKGROUND: Carcinoid tumors are rare neuroendocrine tumors that can be found in the gastrointestinal tract as well as other areas throughout the body.
Rebecca Lapides   +3 more
doaj   +1 more source

International trends in pulmonary neuroendocrine cancer studies:a scientometric study

open access: yesEinstein (São Paulo), 2022
Introduction Pulmonary neuroendocrine tumors account for approximately 20% of all primary lung tumors. Few studies summarize the current body of pulmonary neuroendocrine tumors studies worldwide.
Hugo Tanaka, Auro del Giglio
doaj   +1 more source

Duodenal carcinoid tumour – a case report [PDF]

open access: yes, 2020
Duodenal carcinoids are rare tumours of the small intestine with heterogenous clinical and pathological characteristics. The long-term prognosis is very good if discovered in the early stages.
Alexescu, Teodora Gabriela   +7 more
core   +2 more sources

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