Pancreatitis - classification, etiology, pathogenesis, and clinical manifestations.
Pancreatitis is inflammation of the pancreas, which can be acute (sudden, reversible) or chronic (progressive, leading to irreversible damage and fibrosis).
Classification
- 1 Acute pancreatitis
- Sudden inflammation, potentially reversible.
- May be mild (edematous) or severe (necrotizing).
- 2 Chronic pancreatitis
- Progressive inflammatory disease.
- Leads to permanent structural damage, exocrine and endocrine dysfunction.
Etiology
Acute pancreatitis
- Gallstones (most common cause in many countries).
- Alcohol abuse (second most common).
- Hypertriglyceridemia.
- Hypercalcemia.
- Drugs (e.g., azathioprine, valproic acid).
- Post-ERCP (endoscopic retrograde cholangiopancreatography).
- Trauma.
Chronic pancreatitis
- Long-term alcohol abuse (most common).
- Recurrent acute pancreatitis.
- Genetic mutations (e.g., PRSS1 in hereditary pancreatitis).
- Obstructive causes (e.g., strictures, tumors).
Pathogenesis
Acute pancreatitis
- Premature activation of pancreatic proenzymes (e.g., trypsinogen → trypsin) inside pancreatic acinar cells.
- Activated enzymes cause autodigestion of pancreatic tissue.
- Inflammatory response → interstitial edema, fat necrosis, hemorrhage.
- Systemic inflammatory response syndrome (SIRS) → possible multi-organ failure.
Chronic pancreatitis
- Repeated episodes of pancreatic inflammation.
- Progressive replacement of pancreatic parenchyma with fibrous tissue.
- Loss of exocrine function (malabsorption) and endocrine function (diabetes).