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166 Cards in this Set

  • Front
  • Back
What is the most common tumor of the salivary glands?
pleomorphic adenoma (benign, painless, movable, recurs)
heterotopic salivary gland tissue trapped in a lymph node, surrounded by lymphatic tissue
Warthin's tumor (benign)
What is the most common malignant salivary gland tumor?
mucoepidermoid carcinoma
What causes esophageal dysmotility associated with CREST syndrome?
low pressure proximal to LES
What plexus is lost in achalasia?
myenteric (Auerbach's plexus)
heartburn and regurgitation
nocturnal cough and dyspnea
GERD
painless bleeding of submucosal veins in lower 1/3 of esophagus
Esophageal varices
painful mucosal lacerations at the GE junction due to severe vomiting
hematemesis
associated with alcoholics and bulimics
Mallory-Weiss syndrome
Transmural esophageal rupture due to violent retching
Bowehaave syndrome
Associated with lye ingestion and acid reflux
esophageal strictures
Associated with reflux, infection (HSV-1, CMV, Candida), or chemical ingestion
esophagitis
dysphagia
glossitis
microcytic, hypochromic anemia
predisposes to squamous cell carcinoma
Plummer-Vinson syndrome
(dysphagia due to esophageal webs in proximal 2/3 of esophagus)
What is the metaplasia of Barrett's esophagus?
nonkeratinized (stratified) squamous --> intestinal (columnar) epithelim in distal esophagus
What type of esophageal cancer is most common worldwide?
squamous cell carcinoma
What are the risk factors for esophageal cancer?
Alcohol/achalasia
Barret's
Cigarettes
Diverticuli (Zenker's)
Esophageal web/ esophagitis
Familial
What type of cancer is most common in the head and neck?
squamous cell carcinoma; associated with alcohol and tobacco
Proximal small bowel
diarrhea/ steatorrhea
weight loss
autoantibodies to gliadin
celiac sprue
entire small bowel
diarrhea/ steatorrhea
weight loss
responds to antibiotics
tropical sprue (probably infectious)
Older man with diarrhea/ steatorrhea
PAS-positive macrophages in intestinal lamina propria and mesenteric nodes
Whipple's disease (Tropheryma whippelii)
Older man with diarrhea/ steatorrhea
Arthralgias, cardiac, and neurological symptoms are common
Whipple's disease (Tropheryma whippelii)
Normal villi
Osmotic diarrhea
Occuring after viral enteritis
disaccharidase deficiency
(if virus-induced due to destruction of intestinal villi, it's self-limiting)
Etiologies of:
steatorrhea
vitamin A, D, E, K malabsorption
Pancreatic insufficiency:
cystic fibrosis
pancreatic cancer
obstructing cancer
chronic pancreatitis
Child with steatorrhea, weight loss
Malabsorption and neurologic manifestations
Fat accumulation in enterocytes
Abetalipoproteinemia (decreased synthesis of apo B --> can't generate chylomicrons --> decreased secretion of cholesterol and VLDL into bloodstream --> fat accumulation)
blunted villi
lymphocytes in lamina propria
vesciular rash
Celiac sprue: anti-tissue transglutamiase, anti-gliadin

rash = dermatitis herpetiformis

Moderate increase in risk for T-cell lymphoma,
sloughing of gastric mucosa due to decreased plasma volume --> acute gastritis
Curling's ulcer
increased vagal stimulation --> increased ACh --> increased H+ --> acute gastritis
Cushing's ulcer
macrocytic anemia and achlorhydria
chronic gastritis
pernicious anemia (autoIg to parietal cells)
TYPE A (FUNDUS/BODY) chronic gastritis
caused by H. pylori
increased risk of MALT lymphoma
TYPE B (ANTRUM) chronic gastritis
protein loss
parietal cell atrophy
increased mucous cells
hypertrophied rugae
Menetriere's disease (eldery)
Signet ring cells and acanthosis nigricans
gastric adenocarcinoma
linitis plastica
infiltrative gastric adenocarcinoma
risk factors for gastric adenocarcinoma
associated with smoked foods, achlorhydria, chronic gastritis, type A blood
signet ring cells in both ovaries
Krukenberg's tumor
lymphadenopathy of left supraclavicular node
Virchow's node: mets from
stomach
neck
mediastinum
subcutaneous periumbilical metastasis
Sister Mary Joseph's nodule (gastric cancer)
pain greater with meals --> weight loss
gastric ulcer
pain decreases with meals --> weight gain
duodenal ulcer
causes of gastric ulcers
NSAIDs
H. pylori in 70%
--> decreased mucosal protection against gastric acid
causes of duodenal ulcers
nearly 100% have H. pylori
--> increased gastric acid secretion or decreased mucosal protection
hypertrophy of Brunner's glands
punched-out margins
duodenal ulcer
complications of peptic ulcer disease
bleeding,
penetration into pancreas,
perforation,
obstruction
hypothesized etiology of Crohn's v. UC?
Crohn's - disordered response to intestinal bacterial

UC - autoimmune
Skip lesions
Usually involves terminal ileum and colon
Rectal sparing
Crohn's disease
Continuous colonic lesions including the rectum
UC
Transmural inflammation
Crohn's
Cobblestone mucosa
Crohn's
Creeping fat
Crohn's
Bowel wall thickening ("string sign on barium swallow)
Crohn's
Noncaseating granulomas and lymphoid aggregates
Crohn's
Strictures, fistulas, perianal disease, malabsorption, mutritional depletion
Crohn's
Diarrhea that may or may not be bloody
Crohn's
Migratory polyarthritis,
erythema nodosum
ankylosing spondylitis
uveitis
immunologic disorders
Crohn's
Treatment for Crohn's?
corticosteroids
infliximab (anti-TNF-a)
Mucosal and submucosal inflammation only
UC
Friable mucosal pseudopolyps with freely hanging mesentary
UC
Loss of haustra --> "lead pipe" appearance on imaging
UC
Malnutrition
toxic megacolon
colorectal carcinoma
UC
always bloody diarrhea
UC
Associated with pyoderma gangrenosum and primary sclerosing cholangitis
UC
Treatment for UC?
ASA preparations (sulfasalazine)
Infliximab
Colectomy
Pain improves with defacation
Change in stool frequency or appearance

What is the treatment?
Treat symptoms - irritable bowel disease
Diffuse periumbilical pain
Localized pain 1/3 distance from iliac crest to umbilicus
Fever
Nausea
appendicitis

May lead to peritonitis
DDX: ectopic pregnancy, diverticulitis
mucosa and submucosa outpouch where vasa recta perforate muscularis external
often in sigmoid colon
"false"/acquired diverticulum
mucosa, submucosa, and muscularis externa outpouch
"true" diverticulum
vague abdominal discomfort
painless rectal bleeding
low-fiber diet
diverticulosis (increased intraluminal pressure and weak abd wall)
LLQ pain
fever
leukocytosis
pneumaturia
diverticulitis

(pneumaturia from colocesical fistula)
Treatment for diverticulitis?
antibiotics
halitosis
dysphagia
obstruction
Zenker's diverticulum (herniation of mucosal tissue at junction of pharynx and esophagus)
Painless bleeding
Intussusception or volvulus
Obstruction near the terminal ileum
Meckel's diverticulum
2 inches long
2 feet from ileocecal valve
2% of population
Mecke's diverticulum
Meckel's diverticulum is due to presence of what embryonic structure?
vitelline duct or yolk stalk
Causes of bowel telescoping in
- children
- adults
Intussusception
- children: idiopathic or adenovirus
- adults: uncommon - tumor/ mass
Most common site for bowel twisting in elderly
Volvulus: cecum and sigmoid colon
chronic constipation early in life
failure to pass meconium
associated with Down syndrome

Due to?
Failure of neural crest cells to migrate --> lack of plexuses in rectum/colon
early bilious vomiting
"double bubble" (proximal stomach distension)
associated with Down syndrome
duodenal atresia
meconium ileus is a sign of
cystic fibrosis - meconium plug obstructs intestine
more common in preemies
necrosis of intestinal mucosa
possible perforation
colon usually involved but can be anywhere in GI tract
necrotizing enterocolitis
pain after eating
elderly
cramps with bowel movements
blood in stool
decreased bowel sounds
ischemic colitis (commonly at splenic flexure and distal colon)

secondary to hypoperfusion, occlusion
acute pain
recent surgery
well-demarcated necrotic zones
adhesion
GI bleeding from cecum, terminal ileum, ascending colon
older patients
Dx with angiography
angiodysplasia
What are the predicting factors for whether a polyp becomes CRC?
- villous
- adenomatous
- larger
- epithelial dysplasia
most common non-neoplastic polyp
usually in rectosigmoid colon
hyperplastic polyp
sporadic lesion in children < 5 yo
80% in rectum
no malignant potential if isolated
juvenile polyp
multiple juvenile polyps in GI tract
increased risk of adenocarcinoma
juvenile polyposis syndrome
nonmalignant hamartomas
hyperpigmented mouth, lips, hands, genitalia
increases risk of?
Peutz-Jehgers has increased risk of:
CRC
visceral malignances
thousands of pancolonic polyps, always involves rectum

gene mutation?
Familial adenomatous polyposis:
- APC mutation on 5q
- tumor suppressor gene (2 hits)
- autosomal dominant
thousands of pancolonic polyps,
osseous and soft tissue tumors
retinal hyperplasia
Gardner's syndrome
thousands of pancolonic polyps
malignant CNS tumors
Turcot's syndrome

("TURcot, TURban")
non-adenomatous polyps
autosomal dominant
proximal colon always involved

mutation?
HNPCC/Lynch syndrome:

DNA mismatch repair genes
Risk factors for CRC
- IBD
- S. bovis bacteremia
- tobacco
- large villous adenomas
- juvenile polyposis
- Peutz-Jehgers
obstruction
colicky pain
hematochezia
distal colon cancer
dull pain
Fe deficiency anemia
fatigue
proximal colon cancer
tumor marker of CRC?
CEA
"apple core" lesion
CRC
screening for CRC
>50
stool occult blood
colonoscopy
microsatellite instability -->
HNPCC syndrome (mutations in mismatch repair genes)
Chromosomal instability pathway
1. Loss of APC (decreased intercellular adhesion, increased prolif)
2. K-RAS (unregulated intracellular signal transduction)
3. Loss of p53 (increased tumorigenesis)
At what stage of chromosomal instability does an adenoma develop?
carcinoma?
Adenoma - After K-RAS mutation
Carcinoma - After p53 mutation
"dense core bodies" on EM of small intestine (most commonly)
carcinoid tumor
wheezing
right-sided heart murmur
diarrhea
flushing
carcinoid syndrome (sign of metastasis outside of GI tract)
cirrhotic nodules < 3mm, uniform size are typically due to?
metabolic insult:
- alcohol
- Wilson's disease
- hemochromatosis
cirrhotic nodules > 3mm, varied sizes are typically due to?
significant liver injury
- post-infectious
- drug-induced hepatitis
increases risk of HCC
ALT>AST
vital hepatitis
AST>ALT
alcoholic hepatitis
AST only
myocardial infarcion
increased GGT
liver diseases
heavy alcohol consumption
increased alkaline phosphatase
obstructive liver disease (HCC)
bone disease
bile duct disease
increased amylase
acute pancreatitis
mumps
increased lipase
acute pancreatitis
decreased cerulopasmin
Wilson's disease
swollen and necrotic hepatocytes
neutrophilic infiltration
intracytoplasmic eosinophilic inclusions
fatty change
fibrosis around central vein
alcoholic hepatitis
micronodular, irregularly shrunken liver with "hobnail" appearance
sclerosis around central vein
jaundice
hyperbilirubinemia
AST:ALT > 1.5
alcoholic cirrhosis
Risk factors for:
jaundice, hepatosplenomegaly, ascites, polycythemia, hypoglycemia
hepatocellular carcinoma:
HBV
HCV
Wilson's disease
Hemochromatosis
a1-antitrypsin deficiency
alcoholic cirrhosis
aflatoxin in peanuts
tumor marker for HCC
AFP
mottled liver, centrilobular congestion and necrosis --> cardiac cirrhosis
nutmeg liver
DDx for:
- no JVD
- visible abdominal and back veins
- centrilobular congestion and necrosis
- hepatomegaly
- ascites
- abdominal pain
Budd-Chiari syndrome:
- HCC
- polycythemia
- pregnancy
Mode of inheritance for:
- panacinar emphysema
- PAS-positive globules in liver
a1-antitrypsin deficiency: co-dominant
(protein product accumulates in liver)
What type of bilirubin is elevated in neonatal jaundice?
unconjugated bilirubin (immature UDP-glucuronyl transferase)
Treatment for neonatal jaundice
phototherapy (makes bilirubin water soluble)
high conjugated bilirubin
high urine bilirubin
normal or decreased urobilin
hepatocellular jaundice
(hepatitis, cirrhosis, drug reaction)
high conjugated bilirubin
high urine bilirubin
low urine urobilinogen
obstructive jaundice (gallstone)
high unconjugated bilirubin
absent urine bilirubin (acholuria)
high urine urobilinogen
hemolytic jaundice
Elevated unconjugated bilirubin
May be exacerbated by stress
No overt hemolysis
Asymptomatic
Gilbert syndrome
(decreased UDP-glucuronyl transferase or decreased bilirubin uptake)
Treatment for:
Jaundice early in life
Kernicterus
Increased unconjugated bilirubin
Crigler-Najjar type I
(absent UDP-glucuronyl transferase):
- plasmapheresis
- phototherapy
Treatment for Crigler-Najjar Type II
phenobarbital (increases liver enzyme synthesis)
conjugated hyperbilirubinemia
grossly black liver
Dubin-Johnson syndrome
(Rotor's syndrome is milder form)
asterixis
parkinsonism
corneal deposits
decreased ceruloplasmin
cirrhosis
hepatocellular carcinoma
choreiform movements
dementia
hemolytic anemia
Wilson's disease
treatment for Wilson's disease
penicillamine
inheritance of Wilson's disease
autosomal recessive
Where in the brain does copper accumulate in Wilson's disease?
caudate and putamen (---> Parkinsonism)
Fatigue
Diabetes
Micronodular cirrhosis
Dry mouth
Atrophic testes
Dermal despoits/ skin darkening
Arthropathy
Restrictive cardiomyopathy
Hemochromatosis
Hemochromatosis is associated with what HLA subtype?
HLA-A3
Treatment for hemochromatosis?
phlebotomy
deferoxamine
Causes of hemochromatosis?
Primary - autosomal recessive
Secondary - repeated transfusion
Increased ferritin
Increased iron
Decreased TIBC
Increased ferritin saturation
hemochromatosis
DDx:
pruritis
jaundice
dark urine
light stools
hepatosplenomegaly
- secondary biliary cirrhosis
- primary biliary cirrhosis
- primary sclerosing cholangitis
lymphocytic infiltrate and granulomas
increased anti-mitochondrial Ig

associations?
primary biliary cirrhosis

associated with:
CREST
RA
Celiac
concentric "onion skin" bile duct fibrosis
alternating strictures and dilations on ERCP
hypergammaglobulinemia (IgM)

associations?
primary sclerosing cholangitis

associated with:
UC
leads to secondary biliary cirrhosis
What are major etiologies of secondary biliary cirrhosis?
gallstone
biliary stricture
carcinoma of pancreatic head
chronic pancreatitis
fever
jaundice
RUQ pain
cholangitis (Charcot's triad)
stone type associated with obesity
cholesterol
stone type associated with Crohn's
cholesterol
stone type associated with cystic fibrosis
cholesterol
stone type associated with advanced age
cholesterol or pigment
stone type associated with clofibrate
cholesterol
stone type associated with estrogens
cholesterol
stone type associated with multiparity
cholesterol
stone type associated with rapid weight loss
cholesterol
stone type associated with Native American origin
cholesterol
stone type associated with chronic hemolysis
pigment stone
inspiratory arrest on deep palpation of RUQ
cholecystitis (gallbladder inflammation) - positive Murphy's sign
stone type associated with alcoholic cirrhosis
pigment stone
stone type associated with biliary infection
pigment stone
radiopaque stone
pigment stone
radiolucent with 10-20% opaque due to calcification
cholesterol stone
air seen in biliary tree
gallstone ileus (fistula between gallbladder and small intestine obstructing ileocecal valve)
What virus can cause cholecystitis?
CMV
What is the significance of elevated ALP in cholecystitis?
involvement of bile duct
Causes of acute-onset epigastric pain radiating to back, anorexia, nausea
Acute pancreatitis GET SMASHED:
- gallstones
- ethanol
- trauma
- steroids
- mumps
- autoimmune disease
- scorpion sting
- hypercalcemia/ hyperlipidemia
- ERCP
- drugs (sulfa)
DIC
ARDS
diffuse fat necrosis
hypocalcemia
pseudocyst formation
hemorrhage
infection
multiorgan failure

are all possible complications of?
acute pancreatitis
What are the complications of chronic pancreatitis?
pancreatic insufficiency -->
- vitamin deficiency
- steatorrhea
- diabetes mellitus
What type of pancreatitis is associated with alcoholism and pancreatic cancer?
chronic calcifying pancreatitis
CEA and CA-19-9
pancreatic adenocarcinoma
What increases risk of pancreatic adenocarcinoma?
Where is it usually located
African American, Jewish, cigarettes

head of the pancreas
abdominal pain radiating to back
palpable, painless gallbladder
conjugated hyperbilirubinemia
redness and tenderness on palpation of extremities
pancreatic adenocarcinoma
(Trousseau's, Courvoisier's)
colicky pain without jaundice
obstruction of cystic duct