Table 1.
Tumor classification | Tumor type | Clinical significance |
---|---|---|
Pancreatic exocrine tumors (>95%) |
Invasive ductal adenocarcinoma | The most common type of pancreatic exocrine neoplasm. Accounts for more than 80% of cases. Very poor prognosis. |
Acinar carcinoma | Accounts for less than 1% of cases. Fully malignant. 15% of cases are associated with metastatic fat necrosis. Better overall prognosis than ductal adenocarcinoma. | |
Pancreatoblastoma | Accounts for less than 1% of cases. More common in infants and children than in adults. Less aggressive and better prognosis than ductal adenocarcinoma. | |
Variants of ductal adenocarcinoma (adenosquamous, colloid, medullary, undifferentiated, etc.) |
Adenosquamous (4% of cases), colloid (2%), others rare. Most share a similarly poor long-term prognosis, except for colloid carcinoma, which has a somewhat better prognosis. | |
Cystic neoplasm with invasive carcinoma | Intraductal papillary mucinous neoplasm (IPMN) (2-3% of cases), mucinous cystic neoplasm (MCN) (1%), and solid-pseudopapillary neoplasm (SPT) (<1%). Better prognosis than ductal adenocarcinoma. |
|
Pancreatic endocrine tumors (<5%) |
Pancreatic neuroendocrine tumors (PNETs) (glucagonoma, VIPoma, gastrinoma etc.) |
Commonly accompanied by a clinical syndrome due to aberrant hormone production. Fully malignant, with a 45% 10-year survival rate. |