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Carcinoid Neuroendocrine International Conference and Symposium for Physicans and Patients
Mission Statement
Building towards a cure for Neuroendocrine Tumours and Cancers through Research, Education, Awareness and Support.
Vision Statement
To raise the awareness of NeuroEndocrineTumours (NETs) among patients, the general public, and the medical and the research communities by:

(a) providing well-informed support on management and treatment options to all those involved with NETs; and

(b) supporting NET-directed research and better clinical management practices that will achieve an ultimate goal of early accurate diagnosis and best possible treatment for NET patients

<< Patient Booklet Main Page >>
<< Chapter 4
Carcinoid Tumour
Chapter 6 >>
Pheochromocytoma &Paraganglioma

Chapter 5
Pancreatic Endocrine Tumours

Pancreatic endocrine tumours are the second most common neuroendocrine tumours. These tumours start in the pancreas from specialized cells that make hormones like insulin, gastrin, glucagon, and vasoactive intestinal polypeptide (VIP).

Pancreatic tumours that are functional or secreting cause changes in your blood values, which can make you feel sick. Octreotide can be used to block these hormones. When the hormones are blocked, people tend to feel better. Ongoing changes of these medicines is often needed.


Pancreatic tumours can change your blood sugar levels. You may need medicine to help control your levels. If part of your pancreas has been removed, you may need to take pancreatic enzyme capsules to help you digest food. Octreotide may also block pancreatic enzymes that help digest fat. This can result in your stools becoming pale, foul smelling and floating in the toilet. This cancer is very different from the more common pancreatic cancer that comes from the digestive enzyme producing cells.

Pancreas and nearby Organs




About 33 to 50% of pancreatic tumours are non‐functional. This means they do not secrete hormones. Over time, however, they can change and become hormone secreting.

Pancreatic Tumour Symptom Chart




<< Patient Booklet Main Page >>
<< Chapter 4
Carcinoid Tumour
Chapter 6 >>
Pheochromocytoma &Paraganglioma