woman in 50’s, iron def anemia, dysphagia, cervical esophageal web
Plummer-Vinson Syndrome
- increased risk esophageal SCC
pseudomembranous colitis
C. diff
Barrett esophagus major risk factor for what?
esophageal adenocarcinoma
ingestion of hot foods, HPV, chronic tobacco and EtOH use, achalasia, caustic ingestion
esophageal SCC
Cowdry Type A inclusions, eosinophilic intranuclear inclusions, multinuclear squamous cells
HSV esophagitis
artery that supplies the lesser curvature of the stomach
- also supplies posterior stomach near cardioesophageal junction
left gastric A
- anastomoses w/ R gastric (from proper hepatic) and short gastric (from splenic)
artery supplying the pylorus of stomach, proximal duodenum, and head of pancreas
gastroduodenal A
diarrhea, steatorrhea, weight loss/fat malabsorption, joint pain
- foamy macrophages, PAS-positive, gram-positive
Whipple disease (Tropheryma whippelli) - macrophages compress lacteals in the villi of the small intestine, preventing chylomicrons from entering into the lymphatic system
blunted vili w/ T-lymphocytes in epithelium, weight loss, diarrhea, foul smelling stools
- pruritic vesicular rash
celiac disease /w dermatitis herpetiformis
Crohn disease
uniform, micronodular fibrosis of liver
alcoholic cirrhosis
young pregnant female w/abdominal pain, hepatomegaly, portal HTN
Budd-Chiari
- pregnancy or other hyper-coagulable states!!
epigastric pain, jaundice, weight loss, fatigue
pancreatic adenocarcinoma
- pancreatic pain radiates to back
gallstones, primary sclerosing cholangitis, porcelain gallbladder are all risk factors for?
cholangiocarcinoma (rare)
Murphy’s sign
acute cholecystitis
- pain/inflammation of the gallbladder, without distention (unlike Courvoisier’s sign)
NOTE: gallbladder pain refers to the shoulder d/t phrenic nerve dermatome
Trousseau’s syndrome
migratory, recurrent superficial thrombophlebitis
- inflammation of superficial veins
falciform ligament
connects liver to anterior wall of abdomen
enzyme required to conjugate bilirubin
- not quite mature in newborn physiologic jaundice
UDP glucoronyl* transferase
increased total serum bilirubin levels seen with fasting, dehydration, or stress
- high total bili, normal direct/conj bili
Gilbert disease
- benign, hereditary condition due to decrease in UDP glucuronOSYL* transferase activity
autoimmune destruction of biliary tract, middle aged female
primary biliary cirrhosis
elevation of conjugated/direct bili due to defective liver excretion
- grossly black liver
Dubin Johnson syndrome
MEN type 1
RET gene mutation
MEN type 2A
RET gene mutation
MEN type 2B