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65 Cards in this Set

  • Front
  • Back
At what vertebrae level is the bifurcation of the aorta?
L4
At what vertebrae level is the celiac trunk?
T12
What are the three branches of that celiac trunk?
Spenic, left gastric, and common hepatic arteries
What vessels are anastomosing in esophageal varices?
Left gastric vein (portal) and esophageal vein (systemic)
What vessels are anastomosing in caput medusae?
Paraumbilical veins (portal) and the superficial and inferior epigastric veins (systemic)
What vessels are anastomosing in internal hemroids?
Superior rectal vein (portal) and middle and inferior rectal vein (systemic)
What molecules stimulate the secretion of gastrin?
Phenylalanine, tryptophan, and Ca2+
What hormone is responsible for pancreatic secretion and gallbladder secretion?
CCK
In cholelithiasis, pain worsens after fatty food ingestion due to?
CCK production
What stomach illnesses is somatostatin given to treat?
VIPoma, carcinoid tumors, and Zollinger Ellison syndrome
What is a VIPoma?
Non-alpha, non-beta islet cell pancreatic tumor that secretes VIP. Copious diarrhea.
What are the actions of ghrelin?
Increases growth hormone, ACTH, cortisol, and prolactin secretion.
What nerve runs through the parotid gland?
CN VII facial nerve
What activates trypsinogen to trypsin?
Enterokinase/enterpeptidase, an enzyme secreted from the duodenal mucosa
What is the rate limiting step in carbohydrate digestion?
Oligosaccharide hydrolase at the brush border of intestine producing monosaccharides from olgio- and disaccharides.
Which transporter takes up glucose and galactose?
SGLT1 (Na+ dependent) and GLUT-2
Which transporter takes up fructose?
GLUT-5 (facilitated diffusion) and GLUT-2
M cells
Specialized cells that take up antigen in the Peyer's patches of the small intestine.
What is the only significant mechanism for cholesterol excretion?
Bile
What are the components of bile?
Bile salts, phospholipids, cholestrol, bilirubin, water, ions, and copper (except in Wilson's disease)
What is bilirubin conjugated with and by what?
Bilirubin is conjugated with gluconuronate by glucuronyl transferase.
What does bilirubin travel with in the blood?
Albumin
What is bilirubin secreted into the gut as?
Urobilinogen
What gives stool its characteristic color?
Stercobilin, which is how bilirubin is excreted in feces.
What is the most common salivary gland tumor?
Pleomorphic adenoma - most common tumor, painless, movable mass, benign with a high rate of recurrence.
Warthin's tumor
Benign salivary gland tumor; heterotopic salivary gland tissue trapped in a lymph node, surrounded by lymphatic tissue.
What is the most common malignant salivary gland tumor?
Mucoepidermoid carcinoma
Boerhaave syndrome
Transmural esophageal rupture due to violent retching.

Worse than Mallory-Weiss syndrome (which is NOT transmural).
Ingestion of what toxin is associated with esophageal strictures?
Lye
Plummer-Vinson syndrome
Dysphagia (due to esophageal webs), glossitis, and iron deficiency anemia

Increases the chances of squamous cell cancer of the esophagus.
What deficiency is tropical sprue associated with?
Folate
What are the symptoms of Whipple's disease? What is the treatment?
PAS-positive macrophages in intestinal lamina propria, mesenteric nodes. Arthralgias, cardiac and neurologic symptoms are common. Most often occurs in older men.

Treatment is IV antibiotics for 10 days then TMP-SMX for a year.
What can cause pancreatic insufficiency?
Cystic fibrosis, obstructing cancer, or chronic pancreatitis

Causes malabsorption of fat and fat-soluble vitamins (A, D, E, K).
Abetalipoproteinemia
Decreased synthesis of apo B; inability to generate chylomicrons; decreased secretion of cholestrol,VLDL into bloodstream, fat accumulation in enterocytes. Presents in early childhood with malabsorption and neurologic manifestations.

Vitamin E supplementation can help.
What antibodies are present in celiac sprue?
Antibodies against gliadin, tissue transglutaminase, and endomysial
What skin condition is celiac sprue associated with?
Dermatitis herpetiformis
Curling's ulcer
Decrease in plasma volume due to a burn; causes a sloughing of gastric mucosa.

"Burned by a CURLING iron"
Cushing's ulcer
Brain injury causes increased vagal stimulation, increased ACh, and increased H+ secretion, leading to ulcer development.

"Always CUSHIon the brain"
Menetrier's disease
Gastric hypertrophy with protein loss, parietal cell atrophy, and increased mucous cells. Precancerous. Rugae of the stomach are so hypertrophied that they look like brain gyri.
What histology is present with adenocarinoma of the stomach?
Signet ring cells

Can metastasize to the ovaries, which would be a Krukenberg tumor.
Where are diverticula most often found?
Sigmoid colon
Zanker's diverticulum
False diverticulum. Herniation of mucosal tissue at the junction of the pharynx and esophagus. Presenting symptoms: halitosis (due to trapped food particles), dysphagia, obstruction.
What is the most common congenital anomaly of the GI tract?
Meckel's diverticulum
What is the tumor marker for colorectal cancer?
CEA
What type of lesion is seen on barium enema x-ray for
"Apple core" lesion
What are the symptoms of a carcinoid tymor?
Be FDR - Bronchospasm, Flushing, Diarrhea, and Right sided heart murmurs
What is the treatment for esophageal varices?
Beta-blockers - either propanolol or nadolol
What is the treatment for ascites?
Thiazide diuretic and loop diuretic; possibly pericentisis
ALT > AST
Viral hepatitis
AST > ALT
Alcoholic hepatitis
GGT
Increased with various liver diseases; increased with heavy alcohol consumption
Alkaline phosphatase
Increased with obstructive liver disease (hepatocellular carcinoma), bone disease, or bile duct disease
Amylase
Increased in acute pancreatitis and mumps
Lipase
Increased in acute pancreatitis
Decreased ceruloplasmin
Wilson's disease
What is the mechanism behind Reye's syndrome?
Aspirin metabolites decrease beta-oxidation by reversible inhibition of mitochondrial enzyme.
Mallory bodies
Intracytoplasmic eosinophilic inclusions, present in alcoholic hepatitis.
Would there be a JVP in Budd-Chiari syndrome?
No, it only involves the IVC.
What converts conjugated bilirubin into urobilinogen?
Gut bacteria; some unconjugated bilirubin is converted directly into urobilinogen during heme metabolism, however.
What two liver conditions is phenobarbital used to treat?
Gilbert's syndrome and Crigler-Najjar type II; phenobarbital in these cases increases liver enzyme synthesis.
What hereditary hyperbilirubinemia causes a grossly black liver?
Dubin-Johnson syndrome

Rotor's syndrome, also a conjugated bilirubinemia, does not cause the glossy black liver; it is a milder form of Dubin-Johnson
What part of the brain shows degeneration in Wilson's disease?
Basal ganglia
What is the treatment for Wilson's disease?
Penicillamine
What is the treatment for iron accumulation?
Deferoxamine
What is the classic triad of hemochromatosis?
Micronodular cirrhosis, diabetes mellitus, and skin pigmentation