Results 31 to 40 of about 1,457,192 (230)

Tumor-infiltrating neutrophils predict poor survival of non-functional pancreatic neuroendocrine tumor. Supplementary material

, 2020
Supplementary material for the manuscript "Tumor-infiltrating neutrophils predict poor survival of non-functional pancreatic neuroendocrine tumor".
Wen-Quan Wang (8631932), Xian-Jun Yu (8631965), Chun-Tao Wu (8631960), Liang Liu (8631968), He-Li Gao (8631934), Hua-Xiang Xu (8631952), Wang Jiang (8631954), Shuai-Shuai Xu (8631938), Xuan Han (8631949), Tian-Jiao Li (8631946), Wuhu Zhang (8631660), Xuan Lin (8631957), Hao Li (8631953), Long-Yun Ye (8631956), Shuo Li (8631941)   +14 more
core   +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

Pancreatic paraganglioma mimicking pancreatic neuroendocrine tumor

Rare Tumors, 2020
Extra-adrenal paragangliomas are rare tumors arising from the chromaffin cells of the autonomic nervous system. Retroperitoneal paragangliomas may present as a pancreatic mass.
Arezou Abbasi, Kristina M Wakeman, Venu G Pillarisetty   +2 more
doaj   +1 more source

Total Pancreatectomy for Multicentric Cystic Neuroendocrine Tumor of the Pancreas: A Case Report

Diagnostics, 2022
Pancreatic neuroendocrine tumors (PNETs) are uncommon pancreatic neoplasms with malignant potential, heterogeneous clinical behavior, as well as imaging appearance.
Milica Mitrovic-Jovanovic, Nikica Grubor, Stefan Milosevic, Aleksandra Jankovic, Katarina Stosic, Slavenko Ostojic, Aleksandar Ninic, Marjan Micev, Jelena Djokic Kovac   +8 more
doaj   +1 more source

Challenges of drug resistance in the management of pancreatic cancer [PDF]

, 2010
The current treatment of choice for metastatic pancreatic cancer involves single agent gemcitabine or combination of gemcitabine with capecitabine and erlotinib (tyrosine kinase inhibitor).
Naomi Walsh, Martin Clynes, Rizwan Sheikh, Sheikh, Rizwan, O'Connor, Robert A., Robert O’Connor, Ray McDermott, O'Connor, Robert, Clynes, Martin, Walsh, Naomi, McDermott, Ray   +10 more
core   +1 more source

Excision of bilateral pheochromocytomas followed by staged resection of neuroendocrine carcinoma of the pancreas

Journal of Pediatric Surgery Case Reports, 2020
Pheochromocytoma (PCC) and Pancreatic Neuroendocrine tumor (PNET) occurring together have been considered as a spectrum of Von Hippel Lindau (VHL) Syndrome and carries a grave prognosis.
Sandesh V. Parelkar, Rujuta S. Shah, Sanjay N. Oak, Beejal V. Sanghvi, Gayatri Munghate, Satej S. Mhaskar, D.V. Kulkarni, Rahul Kumar Gupta, Kedar P. Mudkhedkar, Deepa P. Makhija, K.K. Khidtta   +10 more
doaj   +1 more source

Solid Pseudopapillary Neoplasm of the Pancreas in Children and Adolescents: Expert Recommendations

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Solid pseudopapillary neoplasm of the pancreas (SPN) is a rare low‐grade malignant exocrine pancreatic tumor, mostly discovered during the second decade of life in females, with a very good prognosis, provided microscopically complete surgical excision is achieved.
Sabine Irtan, Michael Abele, Calogero Virgone, Michaela Kuhlen, Ricardo Lopez‐Almarez, Tal Ben‐Ami, Ewa Bien, Maja Cesen, Malgorzata A. Krawczyk, Andrea Ferrari, Gianni Bisogno, Yves Reguerre, Dominik T. Schneider, Louise Galmiche, Jorg Fuchs, Sarah Braungart, Bilgehan Yalcin, Ines B. Brecht, Daniel Orbach   +18 more
wiley   +1 more source

Mixed Acinar-Neuroendocrine Carcinoma of the Pancreas with Neuroendocrine Predominance

Case Reports in Medicine, 2013
Background. Pancreatic tumors are rare and could arise from either the exocrine (ductal and acinar cells) or the endocrine (neuroendocrine cells) components of the pancreas.
Onyekachi Henry Ogbonna, Marie Carmel Garcon, Kostas N. Syrigos, Muhammad Wasif Saif   +3 more
doaj   +1 more source

Pancreatic neuroendocrine neoplasms: Clinicopathological features and pathological staging.

, 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   +1 more source

Liver organoids: modelling complexity in homeostasis and disease

FEBS Letters, EarlyView.
Studying liver in vitro has been challenging because simple 2D cell cultures fail to capture liver's cellular and architectural complexity. To bridge this gap, scientists increasingly use organoids, 3D liver models which better mimic liver composition and function. This review examines recent advances in liver organoid complexity and realism, discusses
Anna M. Dowbaj, Meritxell Huch
wiley   +1 more source