Results 31 to 40 of about 39,716 (234)

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 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

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

Pan-p63 but not ΔNp63 (p40) expression in undifferentiated carcinoma of the pancreas

Polish Journal of Pathology, 2020
Undifferentiated carcinoma of the pancreas (UC) is a carcinoma without a definitive direction of differentiation. Tumour protein p63 is a regulator of squamous phenotype, which may also be engaged in tumour development.
Łukasz Liszka
doaj   +1 more source

The rare case of a cystic pancreatic neuroendocrine tumor

Autopsy and Case Reports, 2021
The pancreatic neuroendocrine tumors (PanNETs) most commonly present as solid neoplasms; however, very rarely, they may present primarily as cystic neoplasms. Most of the cystic PanNETs are non-secreting tumors, and the radiological features are not well
Tarun Kumar, Brijnandan Gupta, Prasenjit Das, Kumble S. Madhusudhan   +3 more
doaj  

Advances in medical treatment for pancreatic neuroendocrine neoplasms

World Journal of Gastroenterology, 2022
Pancreatic neuroendocrine neoplasms (PanNENs) are rare neoplasms with strong heterogeneity that have experienced an increasing incidence rate in recent years. For patients with locally advanced or distant metastatic PanNENs, systemic treatment options vary due to the different differentiations, grades and stages.
Li, Yuan-Liang, Cheng, Zi-Xuan, Yu, Fu-Huan, Tian, Chao, Tan, Huang-Ying   +4 more
openaire   +2 more sources

A calcitonin-producing pancreatic neuroendocrine neoplasm treated with distal pancreatectomy a lengthy time after a left trisectionectomy for liver metastases: a case report

Surgical Case Reports, 2022
Background Calcitonin-producing pancreatic neuroendocrine neoplasms (PanNENs) are extremely rare. There have been no reports of a patient in whom liver metastases were the presenting finding, and a calcitonin-producing PanNEN was subsequently detected ...
Ryusei Yamamoto, Ryuzo Yamaguchi, Katsushi Yoshida, Masataka Ando, Yoshitaka Toyoda, Aya Tanaka, Kenji Kato   +6 more
doaj   +1 more source

From diagnosis to treatment: navigating the course for pancreatic neuroendocrine neoplasms. [PDF]

Ann Med
Introduction Pancreatic neuroendocrine neoplasms (pNENs) represent an increasingly significant, unique and complex subgroup of neuroendocrine diseases.
Mastnak L, Badovinac D.
europepmc   +2 more sources