Results 251 to 260 of about 186,677 (303)

Pancreatic Intraductal Papillary Mucinous Neoplasm With Invasive Carcinoma Concomitant With Ampullary Neuroendocrine Tumor: A Case Report. [PDF]

Clin Case Rep
Zhang J, Huang J, He X, Sun M, Han X.
europepmc   +1 more source

Rectal Neuroendocrine Tumor With Non-Atypical Mucous Cell Glands: A Case Report. [PDF]

JGH Open
Ishikawa A, Tanaka H, Yamashita K, Oka S, Mii S.   +4 more
europepmc   +1 more source

Pancreatic Perivascular Epithelioid Cell Tumor (PEComa) Mimicking Neuroendocrine Tumor (NET): A Case Report. [PDF]

Cureus
Hung SE, Yu YT.
europepmc   +1 more source

What Is Your Diagnosis? Splenic Mass in an African Pygmy Hedgehog

Veterinary Clinical Pathology, EarlyView.
Gabriela Hartmann, Milena Carolina Paz, Paola Sônego, Ana Carolina Contri Natal, Lívia Surita, Marcele Bettim Bandinelli, Luciana Sonne   +6 more
wiley   +1 more source

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Neuroendocrine Tumors

Gastroenterology Clinics of North America, 2016
Neuroendocrine tumors are increasingly diagnosed, either incidentally as part of screening processes, or for symptoms, which have commonly been mistaken for other disorders initially. The diagnostic workup to characterize tumor behaviour and prognosis focuses on histologic, anatomic, and functional imaging assessments. Several therapeutic options exist
Basuroy, Ron, Srirajaskanthan, Raj, Ramage, John K   +2 more
  +9 more sources

Gastroenteropancreatic Neuroendocrine Tumors

Gastroenterology Clinics of North America, 2022
Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are the most common type of neuroendocrine tumors and are being increasingly identified in clinical practice. The diagnosis, staging, management, and surveillance of GEP-NETs rely heavily on endoscopy, and consequently, it is important for gastroenterologists to have a solid understanding of these
Conrad J, Fernandes, Galen, Leung, Jennifer R, Eads, Bryson W, Katona   +3 more
openaire   +2 more sources

Pancreatic neuroendocrine tumors

Current Problems in Surgery, 2013
Pancreatic neuroendocrine tumors (PNETs) have an incidence of approximately 1 per 100,000 individuals per year, and account for 1–2% of all pancreatic tumors. The annual incidence in the United States is about 3.65 per 100,000 population. Although they may manifest at any age, they most often occur in the fourth to sixth decades of life. Most PNETs are
Geoffrey W, Krampitz, Jeffrey A, Norton
openaire   +4 more sources

Pancreatic Neuroendocrine Tumors

Surgical Pathology Clinics, 2016
Pancreatic neuroendocrine neoplasms include well-differentiated pancreatic neuroendocrine tumors (PanNETs) and neuroendocrine carcinomas (NECs) with well-differentiated PanNETs accounting for most cases. Other pancreatic primaries and metastatic carcinomas from other sites can mimic pancreatic neuroendocrine neoplasms.
Safia N, Salaria, Chanjuan, Shi
openaire   +2 more sources