Pathology of the Exocrine Pancreas Flashcards

1
Q

contents of acinar glands

A
  • acidophilic zymogen granules which contain a variety of digestive enzymes and proenzymes
  • trypsinogen is the main proenzyme
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2
Q

cells that secrete CCK and seretin

A
  • enteroendocrine cells

- secreted into the blood in response to a meal

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3
Q

function of secretin

A
  • stimulates pancreatic duct cells to produce a fluid high in bicarbonate
  • serves to increase the pH and neutralize the acidic chyme entering the duodenum from the stomach
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4
Q

function of CCK

A
  • stimulates pancreatic acinar cells to produce a secretion rich in digestive enzymes, which function optimally at a neutral or slightly alkaline pH
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5
Q

duct of Wirsung

A
  • main pancreatic duct
  • most commonly drains into the duodenum at the ampulla of Vater
  • in most people it merges with the common bile duct proximal to the ampulla
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6
Q

duct of Santorini

A
  • accessory pancreatic duct present in some people

- drains into the duodenum through a minor papilla 2 cm proximal to the ampulla of Vater

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7
Q

function of the sphincter of Oddi

A
  • surrounds the common bile duct and pancreatic duct to control secretions into the duodenum
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8
Q

enzyme that cleaves trypsinogen

A
  • enteropeptidase (brush border enzyme)
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9
Q

only two enzymes that are secreted in their active form

A
  • lipase and amylase
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10
Q

embryologic origin of the duct of Wirsung

A
  • fusion of the ventral duct and distal dorsal duct
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11
Q

embryologic origin of the duct of Santorini

A
  • occasionally the proximal part of the distal duct persists
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12
Q

cause and result of pancreas divisum

A
  • failure of fetal duct of dorsal and ventral pancreatic primordia to fuse
  • as a result, the bulk of the pancreas drains through the dorsal pancreatic duct and the minor papilla (duct of Santorini)
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13
Q

clinical manifestations of pancreas divisum

A
  • relative stenosis cause by bulk pancreatic secretions predisposes patients to development of recurrent and chronic pancreatitis
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14
Q

cause of annular pancreas

A
  • one portion of ventral pancreatic primordium becomes fixed, while the other portion is drawn around the duodenum
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15
Q

symptoms of annular pancreas

A
  • duodenal obstruction
  • gastric distention
  • vomiting
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16
Q

clinical manifestations of CF

A
  • recurrent pulmonary infections causing chronic lung disease
  • pancreatic insufficiency (steatorrhea, malnutrition)
  • hepatic cirrhosis
  • intestinal obstruction
17
Q

genetic transmission of CF

A
  • autosomal recessive

- most common lethal genetic disease affecting whites

18
Q

gene affected in CF

A
  • cystic fibrosis transmembrane conductance regulator (CFTR) gene on chromosome 7
  • cAMP regulated chloride channel located in apical membrane of glandular epithelium
19
Q

presentation of CF

A
  • CF PANCREAS
  • chronic respiratory disease
  • failure to thrive
  • polyps (nasal)
  • alkalosis, metabolic
  • neonatal intestinal obstruction (meconium ileus)
  • clubbing of fingers
  • rectal prolapse
  • electrolytes increased in sweat
  • aspermia / absence of vas deferens
  • sputum S. aureus / P. aeruginosa
20
Q

pulmonary disease in CF

A
  • loss or reduction of chloride secretion into the ducts of respiratory epithelium
  • leads to increased sodium and water reabsorption from the airway resulting in thicker secretions of mucus
  • leads to defective mucociliary action and the accumulation of hyperconnected, viscid secretions and stasis
21
Q

sweat glands in CF

A
  • reabsorption, not secretion, is affected
  • decreased reabsorption of chloride resulting in increased concentrations of sweat chloride excreted onto the skin causing a hypertonic solution to be secreted containing both high sweat chloride and high sodium content
22
Q

GI manifestations in CF

A
  • pancreatic insufficiency/malabsorption
  • lipid soluble vitamin deficiency
  • failure to thrive
  • biliary stasis
23
Q

chief distinction between acute and chronic pancreatitis

A
  • irreversible impairment of pancreatic function

- parenchymal fibrosis is seen in chronic

24
Q

characteristics of serous cystadenomas

A
  • benign but have malignant potential
  • composed of glycogen-rich cuboidal cells surrounding small cysts
  • fluid is clear, thin and straw-colored
  • more common in women
  • surgical resection is curative
25
Q

characteristics of mucinous cystic neoplasms

A
  • almost always in women
  • can be benign, borderline malignant, or malignant
  • present as painless, slow-growing masses
  • cystic spaces are filled with thick mucin
26
Q

characteristics of intraductal papillary mucinous neoplasms (IPMNs)

A
  • produce cysts containing mucin
  • most are malignant but can be benign or borderline malignant
  • more common in men
  • involve the head of the pancreas more than the tail
  • should be resected because of malignant potential
27
Q

two features useful in distinguishing IPMNs from mucinous cystic neoplasms

A
  • IPMNs lack dense stroma

- IPMNs arise in main pancreatic ducts

28
Q

characteristics of pancreatic carcinoma

A
  • primarily a disease of the elderly
  • more common in blacks
  • CAs of the body and tail do not impinge on the biliary tract and hence remain silent for some time
29
Q

symptoms of pancreatic carcinoma

A
  • pain is usually the first symptom

- obstructive jaundice is associated with most cases of carcinoma of pancreatic head - painless jaundice