Acute pancreatitis

Acute pancreatitis

Unit 7 STRX

Unit 7 STRX

Endocrine system anatomy and physiology
Diagnosing sacral somatic dysfunction
Anatomy of the pelvic girdle
Pituitary gland histology
Pituitary tumors: Pathology review
Nervous system anatomy and physiology
Pancreas histology
Anatomy of the abdominal viscera: Pancreas and spleen
Pancreatic secretion
Acute pancreatitis
Gastrointestinal system anatomy and physiology
Anatomy of the pelvic cavity
Anatomy of the male urogenital triangle
Thyroid and parathyroid gland histology
Nerves and lymphatics of the pelvis
Synthesis of adrenocortical hormones
Adrenal gland histology
Pheochromocytoma
Adrenal masses and tumors: Clinical
Anatomy of the abdominal viscera: Kidneys, ureters and suprarenal glands
Thyroid cancer
Thyroid nodules and thyroid cancer: Pathology review
Thyroid nodules and thyroid cancer: Clinical
Toxic multinodular goiter
Anatomy of the abdominal viscera: Blood supply of the foregut, midgut and hindgut
Anatomy of the thyroid and parathyroid glands
Development of the reproductive system
Testicular and scrotal conditions: Pathology review
Testicular torsion
Anatomy and physiology of the male reproductive system
Anatomy clinical correlates: Male pelvis and perineum
Pediatric urological conditions: Clinical
Hypospadias and epispadias
Anatomy of the male reproductive organs of the pelvis
Prostate gland histology
Benign prostatic hyperplasia
Prostate disorders and cancer: Pathology review
Prostate cancer
Testis, ductus deferens, and seminal vesicle histology
Testicular tumors: Pathology review
Anatomy clinical correlates: Female pelvis and perineum
Anatomy of the perineum
Anatomy of the gastrointestinal organs of the pelvis and perineum
Arteries and veins of the pelvis
Congenital TORCH infections: Pathology review
Parathyroid conditions and calcium imbalance: Clinical
Penis histology
Anatomy of the female reproductive organs of the pelvis
Anatomy of the female urogenital triangle
Anatomy and physiology of the female reproductive system
Anatomy of the urinary organs of the pelvis
Cervical cancer: Clinical
Vaginal cancer: Clinical
Cervical cancer: Pathology review
Anal conditions: Clinical
Fallopian tube and uterus histology
Anatomy of the breast
Cervical cancer
Vulvar cancer: Clinical
Ovary histology
Cervix and vagina histology
Mammary gland histology
Premature rupture of membranes: Clinical
Streptococcus agalactiae (Group B Strep)
Perinatal infections: Clinical
Endometriosis
Endometritis
Uterine disorders: Pathology review
Abnormal uterine bleeding: Clinical
Human papillomavirus
Anatomy clinical correlates: Breast
General anesthetics

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Acute pancreatitis is the sudden inflammation and hemorrhaging of the pancreas due to destruction by its own digestive enzymes—a process fittingly called autodigestion.

Most of the time the disease is actually relatively mild, but it can easily become severe, so it's critical to diagnose and treat it quickly.

The pancreas is a long, skinny gland the length of a dollar bill and is located in the upper abdomen, or the epigastric region, behind the stomach.

It plays endocrine roles—for example, alpha and beta cells make hormones like insulin and glucagon that are secreted into the bloodstream, but it also plays exocrine roles— for example, acinar cells make digestive enzymes that are secreted into the duodenum to help digest food.

These pancreatic digestive enzymes break down macromolecules like carbohydrates, lipids and proteins found in food, but these macromolecules are also found in the cells of the pancreas.

To protect the pancreas, the acinar cells manufacture inactive forms of the enzymes called proenzymes, or zymogens.

These zymogens are normally activated by proteases which cleave off a polypeptide chain, which is kind of like pulling the pin on a grenade.

For additional security, the zymogens are kept away from sensitive tissues in storage vesicles called zymogen granules, and are packaged with protease inhibitors that prevent enzymes from doing damage if they become prematurely active.

To digest a meal, these zymogens are released into the pancreatic duct, and delivered to the small intestine where they are activated by the protease trypsin.

Trypsin is a pancreatic digestive enzyme that is produced as the zymogen trypsinogen.

Normally, trypsinogen isn’t activated until it is cleaved by protease enteropeptidase which is found in the duodenum. But if trypsinogen and these zymogens become activated too early, then it can cause acute pancreatitis, and this might happen as a result of any injury to the acinar cells, or anything that prevents the normal secretion of the proenzymes into the duodenum.

The two leading causes of acute pancreatitis are alcohol abuse and gallstones.

With alcohol abuse it goes like this: alcohol increases zymogen secretion from acinar cells while decreasing fluid and bicarbonate production from the ductal epithelial cells. As a result, the pancreatic juices become really thick and viscous, potentially forming a plug that can block the duct.

A blocked duct is bad news because pancreatic juices start backing up, increasing the pressure, and leading to distention of the duct itself.

At the cellular level, one consequence of this is that membrane trafficking becomes chaotic. Zymogen granules might fuse with lysosomes bringing trypsinogen into contact with lysosomal digestive enzymes.

Trypsinogen might then be turned into activated trypsin which begins the cascade of digestive enzyme activation and autodigestion of the pancreas—which is acute pancreatitis.

Alcohol also contributes to pancreatitis in other ways, though, for example, stimulating acinar cells to release inflammatory cytokines which attracts a strong immune reaction.

Neutrophils arrive quickly at the scene, and often release superoxide and their own proteases, which contribute to the problem.

Finally, it’s thought that high consumption and subsequent oxidative metabolism of alcohol may produce enough reactive oxygen species to overwhelm cellular defenses and damage the cells.

With gallstones what happens is that they sometimes get lodged at the sphincter of Oddi which blocks the release of pancreatic juices, which is pretty similar to the alcohol-induced protein plug.

But the causes of acute pancreatitis are varied and most of the important ones can remembered with the mnemonic “I GET SMASHED”: where ‘I’ refers to unknown, or Idiopathic, causes; ‘G’ is obstruction by Gallstones, ‘E’ is Ethanol abuse; ‘T’ is a pancreatic Trauma, which is more likely if the trauma is the result of a puncture injury (like a knife wound not a punch); ‘S’ is the use of Steroids; ‘M’ is an infection of the Mumps virus, ‘A’ is the result of Autoimmune diseases; the second ‘S’ is the result of Scorpion sting—which is probably the most exciting item on this list and one of the more rare causes; ‘H’ is a cheat and stands for both Hypertriglyceridemia and for Hypercalcemia; ‘E’ is trauma from a procedure called an Endoscopic retrograde cholangiopancreatography or ERCP which is a technique used to diagnose and treat various biliary and pancreatic diseases; and finally ‘D’ stands for Drugs, like sulfa drugs, reverse-transcriptase inhibitors, and protease inhibitors.

So in acute pancreatitis, there is pancreatic tissue destruction that results from the proteases and inflammatory response of the body, and this can cause tiny blood vessels to become leaky and sometimes rupture.

Ultimately, all of the extra fluid or edema causes the capsule of the pancreas to swell, and unfortunately there can be some activation of lipases which go on to destroy the fat around the pancreas, or peripancreatic fat.

All of the digestion and bleeding can actually liquify the pancreatic tissue, a process called liquefactive hemorrhagic necrosis.

Sources

  1. "Robbins Basic Pathology" Saunders (2007)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Acute Pancreatitis" The American Journal of Nursing (1935)
  4. "Practice Guidelines in Acute Pancreatitis" The American Journal of Gastroenterology (2006)
  5. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  6. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)