Results 1 to 10 of about 1,700,231 (391)
China Anti-Cancer Association guideline for diagnosis and treatment of neuroendocrine neoplasm (2022 edition) [PDF]
Zhongguo aizheng zazhi, 2022 Neuroendocrine neoplasm (NEN) is a kind of rare tumor that originated from peptidergic neurons and neuroendocrine cells, which has neuroendocrine differentiation and expresses neuroendocrine markers.
Society of Neuroendocrine Neoplasm of China Anti-Cancer Association
doaj +1 more source
Clinical significance of diagnostic laparoscopy on precision staging in advanced gastric cancer [PDF]
Waike lilun yu shijian, 2022 Gastric cancer is the leading cause of cancer-related deaths in human. More than 70% patients present with advanced gastric cancer or with metastasis in clinic.
NIE Mingming, ZHU Zhenggang
doaj +1 more source
Frontiers in Pharmacology, 2021 Introduction: Osimertinib is an oral, third-generation, irreversible epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that selectively inhibits both EGFR-TKI–sensitizing and EGFR T790M resistance mutations.
Haifeng Qin +5 more
doaj +1 more source
Solid pseudopapillary neoplasm of the pancreas
World Journal of Hepatology, 2021 Solid pseudopapillary neoplasms are rare. This article reviews the clinical and pathologic features of solid pseudopapillary neoplasm of the pancreas, including the epidemiology, cytology, molecular pathology, differential diagnosis, treatment, and ...
A. Omiyale
semanticscholar +1 more source
MALAT1 expression is associated with aggressive behavior in indolent B-cell neoplasms
Scientific Reports, 2023 MALAT1 long non-coding RNA has oncogenic roles but has been poorly studied in indolent B-cell neoplasms. Here, MALAT1 expression was analyzed using RNA-seq, microarrays or qRT-PCR in primary samples from clinico-biological subtypes of chronic lymphocytic
Elena María Fernández-Garnacho +17 more
doaj +1 more source
Pancreatic Solid Pseudopapillary Neoplasm: Key Pathologic and Genetic Features.
Archives of Pathology & Laboratory Medicine, 2020 CONTEXT.— Solid pseudopapillary neoplasm of the pancreas is a low-grade malignant tumor generally associated with a good prognosis. Solid pseudopapillary neoplasms show peculiar morphologic features, but sometimes the differential diagnosis with other ...
S. Rosa, M. Bongiovanni
semanticscholar +1 more source
Neuroendocrine neoplasm update: toward universal nomenclature.
Endocrine-Related Cancer, 2020 Neuroendocrine neoplasia is described in almost every tissue, either in the pure endocrine organs, the nerve structures or in the so-called diffuse neuroendocrine system. The current nomenclature contains time-honored widely accepted definitions; however,
G. Rindi, F. Inzani
semanticscholar +1 more source
Clinics in Colon and Rectal Surgery, 2018 AbstractAppendiceal neoplasms are identified in 0.9 to 1.4% of appendiceal specimens, and the incidence is increasing. It has long been professed that neuroendocrine tumors (formerly carcinoids) are the most common neoplastic process of the appendix; recent data, however, has suggested a shift in epidemiology.
Quinton M, Hatch, Erin W, Gilbert
openaire +2 more sources
Sex differences in solid pseudopapillary neoplasm of the pancreas: A population‐based study
Cancer Medicine, 2020 Solid pseudopapillary neoplasm (SPN) of the pancreas is a rare tumor. This study aims to examine the clinicopathological features and surgical treatments of SPN and compare the clinical behavior and prognosis between men and women with SPN.
Jiali Wu +6 more
semanticscholar +1 more source
Tagraxofusp in Blastic Plasmacytoid Dendritic‐Cell Neoplasm
New England Journal of Medicine, 2019 Background Blastic plasmacytoid dendritic‐cell neoplasm (BPDCN) is an aggressive hematologic cancer that is caused by transformed plasmacytoid dendritic cells that overexpress interleukin‐3 receptor subunit alpha (IL3RA or CD123). Tagraxofusp (SL‐401) is
N. Pemmaraju +17 more
semanticscholar +1 more source