نتایج جستجو برای: carcinoid tumors

تعداد نتایج: 181070  

Journal: :The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi 2013
Su Min Hong You Sun Kim Jung Seop Moon Jin Nam Kim Myoung Ki Oh Sun Ok Kwon Seong Yeon Jeong Seong Woo Hong Yun Kyung Kang

BACKGROUND/AIMS Rectal carcinoid tumors can be resected with endoscopy, and it is important to assess their prognostic factors. We evaluated the potential of Ki-67 expression as a prognostic factor in rectal carcinoid tumors. METHODS We retrospectively reviewed the medical records of 37 patients with rectal carcinoid tumors who got endoscopic resection from January 2001 to January 2011 at Inj...

Journal: :Ear, nose, & throat journal 2016
Lester D Thompson

Neuroendocrine neoplasms of the larynx encompass five separate tumors: paraganglioma, typical carcinoid, atypical carcinoid, small cell carcinoma, and large cell neuroendocrine carcinoma. Many synonyms are employed, with well-, moderately, and poorly differentiated neuroendocrine carcinoma commonly applied to the middle three tumors (World Health Organization preferred terminology). Paraganglio...

2013
Rebecca Dobson Malcolm I. Burgess Melissa Banks D. Mark Pritchard Jiten Vora Juan W. Valle Christopher Wong Carrie Chadwick Keith George Brian Keevil Joanne Adaway Joy E. S. Ardill Alan Anthoney Uschi Hofmann Graeme J. Poston Daniel J. Cuthbertson

PURPOSE Metastatic neuroendocrine tumors secrete serotonin and other vasoactive substances that are responsible for carcinoid syndrome and carcinoid heart disease. We sought to evaluate the discriminatory utility of diagnostic biomarkers in determining the presence and severity of carcinoid heart disease in patients with metastatic neuroendocrine tumors. PATIENTS AND METHODS A cross-sectional...

Journal: :American Journal of Roentgenology 1982

Journal: :The Journal of the Japanese Association for Chest Surgery 1988

2012
Tine Gregersen Nanna Holt Henning Gronbaek Ida Vogel Lars J. Jørgensen Klaus Krogh

Neuroendocrine tumors are rare tumors primarily located in the gastrointestinal tract. Goblet cell carcinoid is a rare subgroup of neuroendocrine tumors located in the appendix. Neurofibromatosis type 1 is an autosomal dominant disorder caused by a mutation in the NF1 gene. Patients with neurofibromatosis type 1 have an increased incidence of typical neuroendocrine tumors, but it is unknown if ...

Journal: :Translation 2023

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