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Clinical features

It is unusual for the common exocrine type of pancreatic cancer to cause warning symptoms in the early stages and even with advanced disease there may be a period of mild, non-specific or vague ill health which is not severe enough for medical attention. People with pancreatic cancer tend to be diagnosed when the disease is very advanced and mild symptoms have suddenly turned into rapidly deteriorating poor health, profound fatigue and rapid weight loss. They are likely to have at least one if not several of the symptoms listed below:

Clinical Features of the rare hormone producing Pancreatic Cancers

These tumours of the pancreas present when the tumour is small because of the symptoms caused by the excess hormone production and not with the symptoms of advanced disease described above, sometimes it may be difficult to locate the tumour because it is so small. They are named either for the hormone they produce or simply called ‘islet tumours’.

Insulinomas produce too much insulin causing weakness and loss of energy, there may be repeated hypoglycaemic attacks.

Gastrinomas produce too much of a hormone called gastrin. Gastrin stimulates acid production by the stomach and too much of this hormone leads to over production of gastric acid which leads to very severe gastric and duodenal ulceration, these cause pain, nausea and may lead to significant bleeding from the ulcers in the gut requiring emergency admission to hospital for treatment of blood loss. Severe ulceration due to over production of gastrin is called the Zollinger-Ellison Syndrome.

Somatostatinomas produce too much of a hormone called somatostatin which prevents the release of insulin and enzymes of the exocrine pancreas. Excess somatostatin therefore causes diabetes and steatorrhoea.

VIPomas produce too VIP hormone (vasoactive intestinal peptide hormone). The symptoms are profuse watery diarrhoea, flushing and high blood pressure.

Glucagonomas are usually cancerous, they cause diabetes mellitus and a distinctive rash called necrolytic migratory erythema.

Amended November 2008