نتایج جستجو برای: neuroendocrine

تعداد نتایج: 20927  

Journal: :Diagnostic Pathology 2007
Summer L Nugent Steven C Cunningham Borislav A Alexiev Emily Bellavance John C Papadimitriou Nader Hanna

BACKGROUND Mixed (composite) exocrine-neuroendocrine cell carcinomas are defined as an intimate admixture of neoplastic glandular exocrine and neuroendocrine cell types. Although gastric adenocarcinoma containing a small number of neuroendocrine cells is a relatively frequent occurrence, gastric neoplasms containing equal proportions of both cell types are rare. CASE PRESENTATION We present a...

2017
Jason E Love Kimberly Thompson Mark R Kilgore Maria Westerhoff Claire E Murphy Antonios Papanicolau-Sengos Kinsey A McCormick Veena Shankaran Natalie Vandeven Faith Miller Astrid Blom Paul T Nghiem Steven J Kussick

Objectives CD200 expression has been well studied in hematopoietic malignancies; however, CD200 expression has not been well-characterized in neuroendocrine neoplasms. We examined CD200 expression in 391 neuroendocrine neoplasms from various anatomic sites. Methods Tissue blocks containing pulmonary small cell carcinoma, pulmonary carcinoid, large cell neuroendocrine carcinoma, pancreatic neu...

Journal: :iranian journal of medical sciences 0
n. afshar moghaddam m. nasr

background: certain marker studies have practical importance in the biology of prostate cancer. the purpose of this study was to determine whether the quantification of certain neuroendocrine and proliferative markers obtained during transurethral resection or prostatectomy, would help in the prognostic evaluation of prostatic adenocarcinomas.   methods: the present study was performed on sampl...

Journal: :Gut 1996
C Bartz C Ziske B Wiedenmann K Moelling

Neuroendocrine pancreatic tumours grow slower and metastasise later than ductal and acinar carcinomas. The expression of the p53 tumour suppressor gene in pancreatic neuroendocrine tumour cells is unknown. Pancreatic neuroendocrine cell lines (n = 5) and human tumour tissues (n = 19) were studied for changed p53 coding sequence, transcription, and translation. Proliferative activity of tumour c...

2016
Takeshi Ito Daisuke Matsubara Ichidai Tanaka Kanae Makiya Zen‐ichi Tanei Yuki Kumagai Shu‐Jen Shiu Hiroki J. Nakaoka Shumpei Ishikawa Takayuki Isagawa Teppei Morikawa Aya Shinozaki‐Ushiku Yasushi Goto Tomoyuki Nakano Takehiro Tsuchiya Hiroyoshi Tsubochi Daisuke Komura Hiroyuki Aburatani Yoh Dobashi Jun Nakajima Shunsuke Endo Masashi Fukayama Yoshitaka Sekido Toshiro Niki Yoshinori Murakami

YAP1, the main Hippo pathway effector, is a potent oncogene and is overexpressed in non-small-cell lung cancer (NSCLC); however, the YAP1 expression pattern in small-cell lung cancer (SCLC) has not yet been elucidated in detail. We report that the loss of YAP1 is a special feature of high-grade neuroendocrine lung tumors. A hierarchical cluster analysis of 15 high-grade neuroendocrine tumor cel...

2014
Stefano La Rosa Daniela Furlan Francesca Franzi Paolo Battaglia Milo Frattini Elena Zanellato Alessandro Marando Nora Sahnane Mario Turri-Zanoni Paolo Castelnuovo Carlo Capella

Sinonasal intestinal-type adenocarcinomas (ITACs) are rare neoplasms histologically resembling intestinal adenocarcinomas. Although a neuroendocrine differentiation in ITACs has been described, true mixed exocrine-neuroendocrine carcinomas, neoplasms in which each component represents at least 30 % of the lesion, are extremely rare and their molecular alterations are largely unknown. We describ...

2012
Qingfu Zhang Jian Ming Siyang Zhang Xueshan Qiu

Neuroendocrine tumors are a heterogeneous group of neoplasms that arise from neuroendocrine cells. Primary renal neuroendocrine tumors are among the most unusual of all renal neoplasms, since neuroendocrine cells are not found within normal renal parenchyma. Here, a case of primary micro neuroendocrine tumor (about 4.7 mm*2 mm) arising in the horseshoe kidney with a cyst of a 45-year-old man wa...

2009
Kyoung-Won Yoon Chang-Hwan Park Wan-Sik Lee Young-Eun Joo Hyeun-Soo Kim Sung-Kyu Choi Jong-Sun Rew Jae-Hyug Lee

Primary neuroendocrine carcinoma of the gallbladder is extremely rare because normal gallbladder mucosa does not contain neuroendocrine cells. Neuroendocrine cells can be detected at sites of intestinal metaplasia induced by chronic inflammation, which may be the initial step in the development of neuroendocrine tumor of the gallbladder. Anomalous union of the pancreaticobiliary duct (AUPBD) is...

Journal: :The Permanente journal 2015
Ahmed Dehal Sean Kim Aamna Ali Thomas Walbolt

Neuroendocrine tumors are either epithelial or neural in origin. Neuroendocrine tumors of the retroperitoneum are mostly metastatic. Primary epithelial neuroendocrine tumors of the retroperitoneum are exceedingly rare. We describe a case of a retroperitoneal tumor that was discovered incidentally during exploratory laparotomy for small-bowel obstruction. Histopathologic and immunochemical analy...

2015
Andrea Celotti Giuseppe Pulcini Mattia Schieppati Silvia Ministrini Alfredo Berruti Maurizio Ronconi

Neuroendocrine tumours (NETs) are a family of neoplasms that come from neuroendocrine cells and express neural markers, such as synaptophysin or chromogranin A.The current classifications of these tumours are presented by the WHO 2000 classification, based on histological parameters, and the WHO 2010 classification, based on the proliferative index, that divides the NETs into a neuroendocrine t...

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