GI 3 Flashcards

(112 cards)

1
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Cirrhosis

Shrunken, atrophic liver (scarring then liver tries to regenerate, forming nodules)

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2
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Cirrhosis

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3
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Cirrhosis

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4
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Cirrhosis

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5
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Cirrhosis

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6
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Cirrhosis

Blue collagen bands in trichome stain

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7
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Cirrhosis

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8
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Steatosis

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9
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Steatosis

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10
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Steatosis

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11
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Steatosis

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12
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Alcoholic Hepatitis

Typically involves neutrophils that infiltrate lobules

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13
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Alcoholic Hepatitis

Arrow: Mallory body

Aggregate of inflammatory cells *largely neutrophils

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14
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Alcoholic Hepatitis Mallory Body

Eosinophilic inclusion, composed mostly of filaments caused by damage to filaments to form cytokeratin

*EXAM*

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15
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Alcoholic Hepatitis

Mallory Hyaline Body

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16
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Alcoholic Liver Disease

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17
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Viral Hepatitis

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18
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Viral Hepatitis (Hemorrhagic)

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19
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Acute Viral Hepatitis

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20
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21
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Viral Hepatitis

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22
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Viral Hepatitis

Acidophilic (Councilman) body (arrow)

A hepatocyte undergoing apoptosis

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23
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Viral Hepatitis

Balloon hepatocytes that are degrading

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24
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Viral Hepatitis B

Ground glass change - cytoplasm turns into smooth ground glass appearance due to viral replication

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25
Viral Hepatitis
26
Viral Hepatitis
27
Hemochromatosis
28
Hemochromatosis Excessive hemosiderin stores
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Hemochromatosis
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Hemochromatosis
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Hemochromatosis
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Hepatocellular Carcinoma
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Hepatocellular Carcinoma Small tumors at periphery
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Hepatocellular Carcinoma
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Hepatocellular Carcinoma
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Metastatic Carcinoma
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Metastatic Carcinoma
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Metastatic Carcinoma
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Metastatic Carcinoma
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Metastatic Carcinoma
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Metastatic Carcinoma
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Cholelithiasis
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Cholelithiasis
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Cholelithiasis
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Cholelithiasis
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Cholelithiasis (Pigment Gallstones) Indicative of chronic hemolysis
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Choledocholithiasis
48
Acute cholecystitis
49
Acute cholecystitis PMNs infiltrating mucosa
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Chronic Cholecystitis
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Chronic Cholecystitis
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Chronic cholecystitis
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Porcelain gallbladder
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Porcelain Gallbladder
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Adenocarcinoma of GB
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Adenocarcinoma of GB
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Adenocarcinoma of GB
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Acute Pancreatitis
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Acute Pancreatitis
60
Acute Pancreatitis
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Acute Pancreatitis White foci= fat necrosis due to fat digestion by lipase, releasing fatty acids that bind to calcium forming soaps (saponification)
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Acute Pancreatitis
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Acute Pancreatitis
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Acute Pancreatitis
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Acute Pancreatitis
66
Chronic Pancreatitis
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Chronic Pancreatitis Concretions and atrophy replaced by chronic scar tissue
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Chronic Pancreatitis Pancreaticpseudocyst (no epithelial lining)
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Chronic Pancreatitis Pancreatic pseudocyst
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Pancreatic Carcinoma
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Pancreatic Carcinoma
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Pancreatic carcinoma
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Pancreatic carcinoma
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PancreaticCarcinoma
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Pancreatic carcinoma
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Pancreatic carcinoma
77
What is the definition of cirrhosis?
Scarring of entire liver with 1) diffuse fibrosis 2) loss of lobular architecture 3) nodular regeneration It is the end-stage of many chronic disorders, so it is difficult to determine precise etiology by histology alone
78
What is the traditional classification of cirrhosis (and its associated diseases)?
Macronodular (\>3 mm) * Viral hepatitis * Alpha-1 antitrypisin deficiency * Wilson's Disease Micronodular (\<3 mm) * Alcoholism * Hemochromatosis * Primary biliary cirrhosis * Wilson's Disease
79
What are some complications of cirrhosis?
Portal HTN Esophageal varices Ascites Splenomegaly Hepatic encephalopathy Hepatocellular carcinoma
80
What is steatosis?
Increased storage of lipid in liver, resulting in yellow appearance (macroscopic) and cytoplasmic vacuoles (microscopic) May be due to variety of causes (alcohol, DM, obesity, protein malnutrition, metabolic disorders)
81
What is alcoholic hepatitis?
Develops in 20-25% of heavy drinks Characterized by: Inflammation and hepatocyte degeneration Neutrophilic infiltrate Steatosis Mallory bodies (eosinophilic PAS +, corkscrew shaped intracytoplasmic stuctures made of intermediate filaments (keratin)
82
What is acute hepatitis characterized by?
Inflammation (mostly lymphocytic, with some neutrophils and eosinophils) Lobular disarray Ballooning degeneration Acidophil (Councilman) bodies May see bridging necrosis (severe cases)
83
How do you distinguish chronic from acute hepatitis?
Distinction from acute made clinically, not pathologically Usually requires elevation of liver enzymes for \>6 months (or persistently elevated viral load)
84
what is hereditary hemochromatosis?
Hereditary hemochromatosis (Bronze diabetes) Autosomal recessive disorder of iron metabolism (HFE gene, chromosome 6p) 1-2/1,000 and M:F = 7:1 (men present earlier in life) Prussian blue stain for iron shows granular staining in hepatocytes
85
How do you distinguish hemochromatosis from secondary hemosiderosis?
Quantitative irone analysis Secondary hemosiderosis = iron overload where iron accumulation typically affects Kupffer cells
86
What are complications of hereditary hemochromatosis?
Cirrhosis Hepatocellular carcinoma Hypopituitarism, skin pigmentation, cardiac failure, DM, arthropathy, testicular atrophy
87
What are predisposing factors for hepatocellular carcinoma (hepatoma)?
Cirrhosis Hep B and C Thorotrast (formerly used as radiographic contrast agent) Alcohol Radiation Alpha-1 antitrypsin deficiency Hemochromatosis
88
What serum marker may be elevated in hepatocellular carcinoma?
Alpha feto-protein
89
What is the macroscopic and microscopic description of hepatocellular carcinoma?
Macro: single/multiple, may have bile staining Micro: Atypical hepatocytes with nuclear pleomorphisms, thickened trabeculae (several layers thick), absent portal tracts
90
What is the prognosis of hepatocellular carcinoma?
Poor 10% 5-year survival
91
What is the most common malignant tumor of the liver?
Metastatic carcinoma
92
What are the most common primary sites for metastatic carcinoma?
GI tract, breast, and lung
93
Describe metastatic carcinoma
Usually multiple circumscribed nodules
94
Describe (macro and micro) the normal gall bladder
Macro: sac-like with thin wall and green mucosal lining Micro: columnar epithelial lining, lamina propria, muscularis propria (no muscularis mucosae or submucosa)
95
What are the types of gallstones
Gallstones occur secondary to supersaturation of bile only 10% of gallstones are pure 1. cholesterol stones: pale, yellow, round/oval, single, radiolucent 2. pigment stones (Ca2+ bilirubinate): black/brown, oval, multiple
96
Risk factors for cholesterol stones
Female, fat, \>40, fertile Drugs GI disorders
97
What are some risk factors for pigment stones?
Chronic hemolysis Certain infections (Bacteria - E. coli; Parasites - Clonorchis) GI disorders
98
How do gallstones form
Secondary to supersaturation of bile
99
What is acute cholecystitis and how is it characterized?
Acute onset of symptoms, 90% associated with gallstones Gallbladder often enlarged, tense Fibrinous serosal exudates May be hemorrhagic, filled with pus, or health with calcification (porcelain GB)
100
What is chronic cholecystitis and how is it characterized?
Recurrent biliary colic or absence of prior acute cholecystitis, virtually always associated with gallstones Wall thickened and fibrotic Chronic inflammation Entrapped epithelial crypts (Rokitansky-Aschoff sinuses)
101
What is an adenocarcinoma of the Gallbladder? - How often does it occur? - Who does it occur in most? - Association with gallstones?
Rare malignancy that is more common in females 80-90% associated with gallstones Most have invaded liver by time of diagnosis Uniformly fatal
102
What is acute pancreatitis associated with?
80% of cases associated with gallstones or alcoholism
103
What is acute pancreatitis characterized by?
Diffuse edema, acute inflammation, hemorrhage, fat necrosis, fibrosis, calcification 20% mortality
104
Pathogenesis of acute pancreatitis
105
What is chronic pancreatitis?
Usually not associated with acute pancreatitis Chronic inflammation, ductal ectasia, squamous metaplasia of ducts, calcification, fibrosis, stone formation, pseudocysts
106
What are some complications of acute pancreatitis?
Systemic organ failure, shock, ARDS, acute renal failure DIC Pancreatic abscess Pancreatic pseudocyst
107
What are some complications of chronic pancreatitis?
Pseudocyst Duct obstruction Malabsorption, steatorrhea Secondary diabetes
108
How common are ductal adenocarcinomas? Where in the pancreas do most of these malignancies occur?
Pretty common 85% of all pancreatic malignancies 2/3 occur in head of pancreas
109
Describe a pancreatic adenocarinoma (macro/microscopically)
Macro: Infiltrative, firm, tan-white tumor Micro: irregular ducts/glands lined by atypical cuboidal to columnar cells, desmoplastic stromal response
110
What are some complications of pancreatic adenocarcinoma?
Primary effects: * Metastases (lung, liver, peritoneum) * Pancreatic carcinoma * Abdominal pain (peripheral lymphatic invasion) Secondary effects: * Trousseau syndrome: Migratory peripheral thrombophlebitis (10-25%) * Courvosier gallbladder: painless jaundice, dilated gallbladder * Weight loss * Obstructive jaundice
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What is the prognosis of pancreatic adenocarcinoma?
\<20% of tumors at diagnosis are surgically resectable Overall poor prognosis: 10% 1-year survival; 2% 5-year survival
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What are some of the mutations associated wth pancreatico adenocarcinoma?
K-Ras, p16, p53, BRCA2, DPC4/SMAD4