Results 1 to 10 of about 111,856 (224)

Recurrent transient visual loss in secretory carcinoid tumor [PDF]

open access: yesAmerican Journal of Ophthalmology Case Reports
Purpose: We describe a case of a 68-year-old woman who had a biopsy-proven carcinoid of the lung and transient episodes of unilateral and bilateral vision loss presumed to be the result to intermittent serum elevations of vasoactive peptides secondary to
Vivian Paraskevi Douglas   +7 more
doaj   +2 more sources

Atelectasis in pediatrics: a case of carcinoid tumor [PDF]

open access: goldRare Tumors, 2017
Carcinoid pulmonary tumors occur in the fourth to sixth decades of life. Usually, typical carcinoid arise a decade earlier when compared to atypical carcinoid (45 years and 55 years, respectively).
Cláudia Guerreiro   +4 more
doaj   +2 more sources

Carcinoid Tumor of the Cecal Appendix. [PDF]

open access: diamondCureus, 2022
Salirrosas Roncal OA   +2 more
europepmc   +3 more sources

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

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   +1 more source

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   +2 more sources

Malignant carcinoid tumor of the pancreas [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2002
Carcinoid tumors arise from argentaffine cells or from a primitive stem cells which may differentiate into anyone of a variety of adult endocrine-secreting cells.
Čolović Radoje B.   +5 more
doaj   +1 more source

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   +2 more sources

An infertile female delivered a baby after removal of primary renal carcinoid tumor

open access: yesOpen Medicine, 2021
Primary renal carcinoid tumors are exceedingly rare. We report a 37-year-old woman with primary infertility, who was found to have a primary renal carcinoid tumor. She became pregnant and gave birth to a baby after removal of the tumor. This is the first
Jhang Syu, Chiu Allen W.
doaj   +1 more source

Complete remission of Cdx-2 positive primary testicular carcinoid tumor: 10-years follow-up and literature review

open access: yesBMC Urology, 2020
Background The neuroendocrine cells can cause a variety of malignancies throughout the human body known as the neuroendocrine tumors (NETs) or carcinoid tumors.
Eugen Widmeier   +2 more
doaj   +1 more source

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