Results 1 to 10 of about 119,598 (183)
Orvosi Hetilap, 2010 The authors review the most important clinical aspects of carcinoid tumors. Carcinoid tumors originating in neuroendocrine cells are rare, usually slowly-growing neoplasms, however, they may present as aggressive and rapidly progressing tumors ...
Bodoky, György +3 more
core +4 more sources
Recurrent transient visual loss in secretory carcinoid tumor [PDF]
American Journal of Ophthalmology Case ReportsPurpose: 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
Carcinoid tumor of the minor papilla in complete pancreas divisum presenting as recurrent abdominal pain [PDF]
BMC Gastroenterology, 2010 Background Tumors of the minor papilla of the duodenum are extremely rare, and they are mostly neuroendocrine tumors, such as somatostatinomas and carcinoid tumors.
Kim Kyeong, Kim Tae, Kim Yong
doaj +3 more sources
Primary carcinoid tumor of the gallbladder: A case report and brief review of the literature [PDF]
World Journal of Surgical Oncology, 2010 Background Primary carcinoid tumor of the gallbladder is rare and comprises less than 1% of all carcinoid tumors. Preoperative diagnosis of carcinoid tumor of the gallbladder is difficult. The imageology findings are similar to those in other gallbladder
Liu Hao-Run +3 more
doaj +3 more sources
Primary carcinoid tumor arising within mature teratoma of the kidney: report of a rare entity and review of the literature [PDF]
Diagnostic Pathology, 2007 Background Primary carcinoid tumor arising within mature teratoma of the kidney is extremely rare, and their clinicopathologic features are not well described.
Parwani Anil V, Armah Henry B
doaj +3 more sources
Thoracic 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
Malignant carcinoid tumor of the pancreas [PDF]
Srpski 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
The 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 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
Duodenal carcinoid tumour – a case report [PDF]
, 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