Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Midgut Carcinoid Tumor"'
Autor:
M.E. Castro-Peraza, Hugo Álvarez-Argüelles, A. Bravo-Gutiérrez, A. Alarcó-Hernández, Antonio Martínez-Riera, J.L. Carrasco-Juan, S. González-García, H. Roldán-Delgado, A.C. Rahy-Martín, V. Medina-Arana
Publikováno v:
International Journal of Colorectal Disease. 31:1561-1563
Dear Editor: Carcinoid tumors are slow-growing neoplasms derived from enterochromaffin cells or Kulchintsky cells being thus neuroendocrine in nature. They may arise anywhere in the gastrointestinal tract, in the bronchi, and occasionally elsewhere (
Autor:
Göran Åkerström, Katarina Edfeldt, Peter Stålberg, Gunnar Westin, Peyman Björklund, Per Hellman
Publikováno v:
Endocrine-Related Cancer. 18:479-489
The genetic events leading the progression of midgut carcinoid tumors are largely unknown. The disease course varies from patient to patient, and there is a lack of reliable prognostic markers. In order to identify genes involved in tumor progression
Autor:
Eva Tiensuu Janson, Janet L. Cunningham, Mats Stridsberg, Staffan Welin, Kjell Öberg, Barbro Eriksson, Britt Skogseid, Dan Granberg
Publikováno v:
Neuroendocrinology. 89:302-307
Background: Patients with malignant midgut carcinoids are occasionally diagnosed with limited tumor spread, and surgery with radical intention is performed. Despite curative intent, recurrences occur frequently, motivating long-term biochemical and r
Autor:
Fan Fan, Michael J. Gray, Ray Somcio, Wenbiao Liu, George Van Buren, E. Ramsay Camp, Anthony D. Yang, Eddie K. Abdalla, Lee M. Ellis, Asif Rashid, James C. Yao
Publikováno v:
Clinical Cancer Research. 13:4704-4712
Purpose: Gastrointestinal neuroendocrine tumors (NET) are rare heterogeneous tumors that hypersecrete neuropeptides. The scarcity of good gastrointestinal NET models has limited the ability to study potential therapeutic agents. We describe and chara
Publikováno v:
The Journal of the American Association of Gynecologic Laparoscopists. 10:127-130
Chronic pelvic pain is common in women of reproductive age and accounts for more than 40% of all laparoscopic procedures. In up to 40% of these patients laparoscopic findings are negative. As a result, many gynecologists frequently excise portions of
Death resulting from low-grade midgut carcinoid tumor: Autopsy findings and review of the literature
Publikováno v:
Archives of International Surgery. 7:111
Autor:
Claudio Pasquali, Sergio Pedrazzoli, Lucia Moletta, Rita Alaggio, Valbona Liço, Anna Caterina Milanetto
s / Pancreatology 14 (2014) S1eS129 S80 Conclusion: CSE inhibits pancreatic ductal fluid secretion and the activity of the CFTR which may play role in the smoke-induced pancreatic damage. This study was supported by OTKA, MTA and NFU/T AMOP.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c1400a0c6a8ea95f5411d01f5b22e90
http://hdl.handle.net/11577/3226826
http://hdl.handle.net/11577/3226826
Autor:
Håkan Ahlman, Lars Kölby, Eva Forssell-Aronsson, Bo Wängberg, Göran Stenman, Bo Ahrén, Sven Karlsson, A. Wigander, Viktor Johanson, Peter Bernhardt, Ola Nilsson
Publikováno v:
The American Journal of Pathology. 158:745-755
A human midgut carcinoid tumor was successfully transplanted into nude mice and propagated for five consecutive generations (30 months) with well-preserved phenotype. Tumor cells in nude mice expressed identical neuroendocrine markers as the original
Publikováno v:
Neurochemical Research. 22:977-983
Hormonal overproduction is a significant problem in patients with disseminated midgut carcinoid tumors. Serotonin (5-HT) is one major product secreted from such tumors and the urinary excretion of its metabolite (5-hydroxyindoleacetic acid, 5-HIAA) s
Autor:
S. Porcel Carreño, M Alvarado Arenas, E Rodríguez Martín, C Fletes Peral, J.A. Riesco Miranda, A. Rodríguez Trabado, S Jiménez Timón, J Hernández Arbeiza, R. Cobo López
Publikováno v:
Allergologia et Immunopathologia. 32:235-237
Background The association of bronchial carcinoid tumours with carcinoid syndrome is extremely rare especially in the absence of metastasic disease, and the angioedema is not a typical sign of this syndrome Methods and results We report the case of a