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Related Concept Videos

Chronic Pancreatitis I: Introduction01:25

Chronic Pancreatitis I: Introduction

Chronic pancreatitis is a long-standing, relapsing inflammation of the pancreas, characterized by irreversible damage to the gland. It results in progressive destruction of the pancreatic parenchyma, fibrosis, and eventual loss of both exocrine and endocrine function. The disease may evolve gradually after multiple episodes of acute pancreatitis or develop independently.EtiologyChronic pancreatitis can arise from a variety of causes:Alcohol use is the leading cause, accounting for 70–80% of...
Chronic Pancreatitis I: Introduction01:24

Chronic Pancreatitis I: Introduction

The pancreas, an elongated and flat gland situated behind the stomach, serves a vital function in digesting food and managing blood sugar levels.
Pancreatitis is the inflammation of the pancreas, which occurs when the immune system becomes active and causes swelling, pain, and disruptions in organ function. Pancreatitis can manifest as either an acute or chronic condition.
Acute pancreatitis arises suddenly and lasts for a brief duration, while chronic pancreatitis is a long-term affliction...
Chronic Pancreatitis II: Pathophysiology01:21

Chronic Pancreatitis II: Pathophysiology

Chronic pancreatitis is a progressive and irreversible inflammation of the pancreas, most often caused by long-term alcohol abuse, but it can also be related to ductal obstruction, smoking, or genetic factors.Chronic pancreatitis occurs when the pancreas is repeatedly exposed to harmful agents like alcohol, smoking, ductal obstruction, or genetic predisposition. These factors lead to the release of toxic metabolites and inflammatory cytokines, sustaining chronic inflammation in the pancreatic...
Acute Pancreatitis I: Introduction01:25

Acute Pancreatitis I: Introduction

Acute pancreatitis is the sudden inflammation of the pancreas caused by the early activation of digestive enzymes, leading to the autodigestion of pancreatic tissue. This results in local inflammation and, in severe cases, systemic complications.EtiologyUnderstanding the underlying causes is crucial, as identifying the etiology guides treatment and anticipates complications. Acute pancreatitis can be triggered by various factors, typically grouped into the following clinical categories.Biliary...
Acute Pancreatitis I: Introduction01:27

Acute Pancreatitis I: Introduction

Pancreatitis is inflammation of the pancreas, an organ located behind the stomach. It can be either acute or chronic.
Acute pancreatitis is characterized by rapid inflammation of the pancreas, often caused by factors like gallstone blockage or excessive alcohol consumption. Chronic pancreatitis, on the other hand, is a slow, progressive inflammation that may result from long-term alcohol abuse, obstructions in the pancreatic duct, or genetic factors.
The causes of acute pancreatitis include:
Acute Pancreatitis II: Pathophysiology01:21

Acute Pancreatitis II: Pathophysiology

The pathophysiology of acute pancreatitis centers on injury to pancreatic acinar cells, which initiates a cascade of harmful intracellular events.This injury leads to premature activation of trypsinogen to trypsin in the pancreas. Trypsin then activates other digestive enzymes, such as chymotrypsin, elastase, and phospholipase A2, which begin breaking down pancreatic tissue. The resulting autodigestion causes local inflammation, tissue swelling, hemorrhage, and fat necrosis.Injured acinar cells...

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Related Experiment Video

Updated: Jun 24, 2026

A Simple and Rapid Method for Simultaneous Isolation of Primary Islets and Primary Pancreatic Acinar Cells from Mice
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Autoimmune pancreatitis: an update.

Aravind Sugumar1, Suresh Chari

  • 1Mayo Clinic College of Medicine, Division of Gastroenterology and Hepatology, 200 First St SW, Rochester, MN, USA. sugumar.aravind@mayo.edu

Expert Review of Gastroenterology & Hepatology
|April 9, 2009
PubMed
Summary
This summary is machine-generated.

Autoimmune pancreatitis (AIP) is a rare systemic fibroinflammatory disorder affecting the pancreas and potentially other organs. Early diagnosis and differentiation from pancreatic cancer are crucial for effective steroid treatment and management of relapses.

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Last Updated: Jun 24, 2026

A Simple and Rapid Method for Simultaneous Isolation of Primary Islets and Primary Pancreatic Acinar Cells from Mice
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Area of Science:

  • Gastroenterology
  • Immunology
  • Oncology

Background:

  • Autoimmune pancreatitis (AIP) is a distinct clinical entity recently recognized as a pancreatic manifestation of a systemic fibroinflammatory disorder.
  • AIP can involve multiple organs, including bile ducts, salivary glands, kidneys, and lymph nodes, presenting synchronously or metachronously.
  • This condition predominantly affects males in their fifth and sixth decades, with obstructive jaundice as a common, though often nonspecific, symptom.

Purpose of the Study:

  • To summarize the current understanding of autoimmune pancreatitis (AIP).
  • To highlight diagnostic criteria and the importance of differentiating AIP from pancreatic cancer.
  • To discuss the therapeutic response to steroids and the management of relapses.

Main Methods:

  • Diagnosis relies on established criteria combining clinical presentation, imaging (CT, MRI, ERCP), serology, pancreatic histology, and response to steroids.
  • Differentiating AIP from pancreatic cancer is critical due to distinct prognoses and treatments.
  • Monitoring disease progression and response to treatment.

Main Results:

  • AIP responds dramatically to steroid treatment.
  • Relapses are common but often responsive to re-treatment with steroids.
  • Increasing clinical experience is improving the understanding of AIP's natural history.

Conclusions:

  • Autoimmune pancreatitis requires careful diagnosis and differentiation from pancreatic cancer.
  • Steroid therapy is effective for AIP, but relapse management is essential.
  • Continued research and clinical observation are vital for a comprehensive understanding of AIP.