Results 11 to 20 of about 393,422 (164)

Surgical management of pancreatic neuroendocrine neoplasms [PDF]

Laparoscopic, Endoscopic and Robotic Surgery, 2023
Pancreatic neuroendocrine neoplasms are a rare and complex group of neoplastic lesions that develop from pancreatic islet cells. Their incidence has dramatically increased during the last two decades.
Piero Alberti, David Martin, Georgios Gemenetzis, Rowan Parks   +3 more
doaj   +4 more sources

Pancreatic neuroendocrine neoplasms: Clinicopathological features and pathological staging. [PDF]

, 2020
The nomenclature and classification of pancreatic neuroendocrine neoplasms has evolved in the last 15 years based on the advances in knowledge of the genomics, clinical behaviour and response to therapies.
Lam, Alfred King-Yin, Ishida, Hirotaka
core   +2 more sources

Expression studies on PPARγ in pancreatic neuroendocrine tumours [PDF]

, 2010
MDPancreatic NETs occur with an annual incidence of around 5 per 1,000,000 population per year, with survival rates of between 30 – 97% at 5 years depending on the tumour subtype.
Hanson, Matthew Richard
core   +4 more sources

Neuroendocrine Neoplasms

, 2022
Pancreatic neuroendocrine neoplasms (PanNENs) are tumors with neuroendocrine differentiation and are divided into functioning (syndromic) or non-functioning based on the clinical syndromes. Insulinomas are the most common functioning NETs.
Maria Gaia Mastrosimini, Lavinia Stefanizzi, Stefano Gobbo, Paola Capelli, Paolo Tinazzi Martini, Aldo Scarpa, Mirko D’Onofrio, Riccardo De Robertis, Alessandro Beleù, Luca Geraci   +9 more
core   +1 more source

Development and validation of a simple-to-use nomogram to predict liver metastasis in patients with pancreatic neuroendocrine neoplasms: a large cohort study

BMC Gastroenterology, 2021
Background Liver metastasis is an important prognostic factor for pancreatic neuroendocrine neoplasms (pNENs), but the relationship between the clinical features of patients with pNEN and liver metastasis remains undetermined.
Maoen Pan, Yuanyuan Yang, Tianhong Teng, Fengchun Lu, Yanchan Chen, Heguang Huang   +5 more
doaj   +1 more source

Pancreatic neuroendocrine tumor with complete replacement of the pancreas by serous cystic neoplasms in a patient with von Hippel-Lindau disease: a case report

Surgical Case Reports, 2017
Background von Hippel-Lindau disease is a dominantly inherited multi-system syndrome with neoplastic hallmarks. Pancreatic lesions associated with von Hippel-Lindau include serous cystic neoplasms, simple cysts, and neuroendocrine tumors. The combination
Shimpei Maeda, Fuyuhiko Motoi, Shuhei Oana, Kyohei Ariake, Masamichi Mizuma, Takanori Morikawa, Hiroki Hayashi, Kei Nakagawa, Takashi Kamei, Takeshi Naitoh, Michiaki Unno   +10 more
doaj   +1 more source

Chinese expert consensus on multidisciplinary diagnosis and treatment of pancreatic neuroendocrine liver metastases

Journal of Pancreatology, 2023
Many management strategies are available for pancreatic neuroendocrine neoplasms with liver metastases. However, a lack of biological, molecular, and genomic information and an absence of data from rigorous trials limit the validity of these strategies ...
Yihebali Chi, Liming Jiang, Susheng Shi, Shun He, Chunmei Bai, Dan Cao, Jianqiang Cai, Qichen Chen, Xiao Chen, Yiqiao Deng, Shunda Du, Zhen Huang, Li Huo, Yuan Ji, Jie Li, Wenhui Lou, Jie Luo, Xueying Shi, Lijie Song, Bei Sun, Huangying Tan, Feng Wang, Xuan Wang, Zhewen Wei, Wenming Wu, Dianrong Xiu, Jianming Xu, Huadan Xue, Yi Yang, Fei Yin, Jiangyuan Yu, Chunhui Yuan, Yefan Zhang, Weixun Zhou, Dongbing Zhao, Hong Zhao   +35 more
doaj   +1 more source

Pancreatic mixed acinar-neuroendocrine carcinoma with intraductal growth: A case report with radiologic–pathologic correlations

Radiology Case Reports, 2023
Pancreatic mixed acinar-neuroendocrine carcinomas are rare malignant tumors of the pancreas. They are composed histologically of both acinar and neuroendocrine cells.
Hiroshi Baba, MD, Yasunari Yamada, MD, Kazuhiro Tada, MD, Yusuke Kuboyama, MD, Kengo Fukuzawa, MD, Kentaro Iwaki, MD, Mitsuteru Motomura, MD, Ryo Takaji, MD, Ryuichi Shimada, MD, Hajime Takaki, MD, Yoshiki Asayama, MD   +10 more
doaj   +1 more source

Tuberous Sclerosis Complex With Multiple Organ Tumors: Case Report and Literature Review

Frontiers in Oncology, 2022
Pancreatic neuroendocrine neoplasms (PNEN) are tumors that originate from neuroendocrine cells. Only about 1% patients are related to mutation of tuberous sclerosis complex gene. Here, we reported a rare case with involvement of multiple organs and space-
Xinhe Zhang, Xinping Zhong, Xuyong Lin, Xuedan Li, Haoyu Tian, Bing Chang, Ying Wang, Jing Tong, Ningning Wang, Dan Li, Xiuli Jin, Die Huang, Yanmeng Wang, Huipeng Cui, Lin Guan, Yiling Li   +15 more
doaj   +1 more source

Increased neutrophil–lymphocyte ratio predicts recurrence in patients with well-differentiated pancreatic neuroendocrine neoplasm based on the 2017 World Health Organization classification

BMC Surgery, 2021
Background The prognostic values of inflammation-based markers in well-differentiated pancreatic neuroendocrine neoplasms, diagnosed according to the new 2017 World Health Organization classification, have remained unclear.
Takayuki Miura, Hideo Ohtsuka, Takeshi Aoki, Shuichi Aoki, Tatsuo Hata, Tatsuyuki Takadate, Shimpei Maeda, Kyohei Ariake, Kei Kawaguchi, Kunihiro Masuda, Masaharu Ishida, Masamichi Mizuma, Kei Nakagawa, Takanori Morikawa, Fumiyoshi Fujishima, Takashi Kamei, Hironobu Sasano, Michiaki Unno   +17 more
doaj   +1 more source