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  2. Pancreatic neuroendocrine tumor - Wikipedia

    en.wikipedia.org/.../Pancreatic_neuroendocrine_tumor

    Pancreatic neuroendocrine tumours (PanNETs, PETs, or PNETs), often referred to as "islet cell tumours", [1] [2] or "pancreatic endocrine tumours" [3] [4] are neuroendocrine neoplasms that arise from cells of the endocrine and nervous system within the pancreas.

  3. Gastrinoma - Wikipedia

    en.wikipedia.org/wiki/Gastrinoma

    Gastrinoma is the second most common functional pancreatic neuroendocrine tumor (pNET), with a yearly incidence of approximately 0.5 to 21.5 cases per a million of people worldwide. [5] Gastrinomas are located predominantly in the duodenum (70%) and pancreas (25%). [20]

  4. Neuroendocrine tumor - Wikipedia

    en.wikipedia.org/wiki/Neuroendocrine_tumor

    Pancreatic neuroendocrine tumors (PanNETs) are often referred to as "islet cell tumors", [54] [55] or "pancreatic endocrine tumors" [4] The PanNET denomination is in line with current WHO guidelines. Historically, PanNETs have also been referred to by a variety of terms, and are still often called "islet cell tumors" or "pancreatic endocrine ...

  5. Primitive neuroectodermal tumor - Wikipedia

    en.wikipedia.org/.../Primitive_neuroectodermal_tumor

    Primitive neuroectodermal tumor is a malignant (cancerous) neural crest tumor. [1] It is a rare tumor , usually occurring in children and young adults under 25 years of age. The overall 5 year survival rate is about 53%.

  6. Insulinoma - Wikipedia

    en.wikipedia.org/wiki/Insulinoma

    Insulinomas are one of the functional pancreatic neuroendocrine tumour (PNET) group ("functional" because it increases production of insulin). [1] In the Medical Subject Headings classification, insulinoma is the only subtype of "islet cell adenoma ".

  7. Pancreatic tumor - Wikipedia

    en.wikipedia.org/wiki/Pancreatic_tumor

    A pancreatic tumor is an abnormal growth in the pancreas. [1] In adults, almost 90% are pancreatic cancer and a few are benign. [1] Pancreatic tumors are rare in children. [1] Classification is based on cellular differentiation (ductal, acinar, neuroendocrine, other) and gross appearance (intraductal, cystic, solid). [1]

  8. Exelixis (EXEL) Q4 2024 Earnings Call Transcript - AOL

    www.aol.com/exelixis-exel-q4-2024-earnings...

    We have pancreatic neuroendocrine tumor, GI neuroendocrine tumor, lung neuroendocrine tumor, functional/non-functional neuroendocrine tumors, and neuroendocrine tumors enrolled regardless of their ...

  9. VIPoma - Wikipedia

    en.wikipedia.org/wiki/VIPoma

    A VIPoma or vipoma (/ v ɪ ˈ p oʊ m ə /) is a rare endocrine tumor [1] that overproduces vasoactive intestinal peptide (thus VIP + -oma). The incidence is about 1 per 10,000,000 per year. VIPomas usually (about 90%) originate from the non-β islet cells of the pancreas. They are sometimes associated with multiple endocrine neoplasia type 1.

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