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PH-GI18

Pancreatic tumours

How pancreatic ductal adenocarcinoma grows from precursor lesions and invades early, why a tumour of the head causes painless jaundice while one in the body or tail is found late, and the cystic and neuroendocrine tumours of the pancreas.

By the end, you can

  • Relate the ducts, acini and islets of the pancreas to the tumours that arise from each.
  • Explain the progression from pancreatic intraepithelial neoplasia to ductal adenocarcinoma and its main genetic changes.
  • Explain why pancreatic cancer invades early and why its site in the gland shapes how it presents.
  • Distinguish the main cystic neoplasms of the pancreas by their lining, contents and malignant potential.
  • Relate functioning pancreatic neuroendocrine tumours to the hormones they secrete.
  • Recognise the classic appearances, resectability categories and tests of pancreatic tumours, and explain how surgery, chemotherapy, enzyme replacement and neuroendocrine treatments act on the mechanism.

What it is

Most pancreatic cancers are pancreatic ductal adenocarcinomas (PDAC): infiltrating, duct-like malignant glands in a dense fibrous stroma, which invade early and are usually advanced when found. The pancreas also gives rise to cystic neoplasms, some benign and some precursors of cancer, to neuroendocrine tumours of the islet cells, which may secrete hormones, and to rarer tumours such as acinar cell carcinoma.

5 types to tell apart
Pancreatic ductal adenocarcinoma
Roughly nine in ten pancreatic cancers; most arise in the head. Infiltrating glands in a dense desmoplastic stroma, with a marked tendency to invade nerves.
Intraductal papillary mucinous neoplasm (IPMN)
A mucin-secreting papillary growth inside the main duct or its branches, which it dilates; involvement of the main duct carries the higher risk of cancer.
Mucinous cystic neoplasm (MCN)
A mucin-filled cyst, almost always in women and in the body or tail, with an ovarian-type stroma and no connection to the ducts; it can progress to carcinoma.
Serous cystic neoplasm
Serous cystadenoma: many tiny cysts lined by glycogen-rich cells, often round a central scar; almost always benign, and associated with von Hippel–Lindau disease.
Pancreatic neuroendocrine tumour (PanNET)
Arises from islet cells; most secrete no hormone, but functioning tumours cause insulin, gastrin, glucagon or VIP excess. Graded 1 to 3 by proliferation; associated with MEN1.

US spelling: tumours → tumors.

Normal function

Ducts, acini and islets

The pancreas lies across the back of the upper abdomen: its sits in the curve of the , its crosses the spine and its reaches the spleen. The runs through the head to join the , and both open at the .

Most of the gland is exocrine. Clusters of acinar cells secrete digestive enzymes into small ducts lined by cuboidal cells that add bicarbonate; the ducts merge into the main duct. Scattered among the acini, the islets of Langerhans (a few per cent of the gland) contain beta cells (insulin), alpha cells (glucagon), delta cells (somatostatin) and others.

Each cell type gives rise to its own tumours: the duct lining to ductal adenocarcinoma and the mucinous cystic tumours, the islet cells to neuroendocrine tumours, and the acinar cells, rarely, to acinar cell carcinoma.

Point to it on the model