Liver, Pancreas Flashcards

(43 cards)

1
Q

acidophilic apoptotic bodies

A

Councilman bodies

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2
Q

Test of Hepatocyte integrity

A

ALT AST LDH

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3
Q

Test for Hepatocyte synthetic function

A

Albumin
PT aPTT
Ammonia

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4
Q

Test of Biliary excretory function

A

Bilirubin
ALP
gamma - glutamyl transpeptidase

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5
Q

MCC of Portal hypertension

A

Cirrhosis 85%

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6
Q

Characteristic of Ascites

A

Serous, <3g/dL protein (mostly albumin)
Serum:ascitic fluid albumin gradient >/1.1g/dL

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7
Q

Hepatitis that can cause severe hepatitis in pregnant

A

HEV

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8
Q

Hepatitis that is more associated with chronic liver disease

A

HCV

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9
Q

Hallmark of chronic viral hepatitis

A

Portal inflammation with fibrosis

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10
Q

Hepatitis C specific findings

A

CaLaBaSa

Lymphoid follicles
Bile duct injury
Steatosis

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11
Q

Specific findings in Hepatitis B

A

Ground Glass hepatocytes

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12
Q

inflammatory cells (lymphocyte and plasma cells) within cytoplasm of hepatocytes

A

Emperipolesis
seen in AI Hepatitis

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13
Q

hepatocellular pattern seen in Drug induced hepatitis

A

centrizonal necrosis

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14
Q

Diagnosis criteria of NASH

A

Steatosis
Lobular inflammation
Ballooned hepatocytes

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15
Q

MCC of chronic liver disease in US

A

Non-alcoholic Fatty Liver disease (NAFLD)
Assoc with Metabolic syndrome

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16
Q

TRIAD of Hemochormatosis

A

Micronodular cirrhosis
DM
Skin pigmentation

Excessive Iron absorption and deposition into liver and pancreas

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17
Q

AD, impaired Cu excretion into bile and incorporation to Ceruloplasmin
ATP7B mutation Ch13
Movement disorder
Kayser-Fleischer rings

A

Wilson Disease
inc tissue Cu, Dec serum ceruloplasmin, inc urinary Cu excretion

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18
Q

MC diagnosed inherited hepatic disorder in infants and children

A

A1 antitrypsin deficiency

19
Q

AR, MRP2 mutation (impaired transport of non-bile salt organic anions at canalicular membrane)
black liver discoloration

A

Dubin-Johnson

20
Q

AR
Impaired STORAGE of conjugated bilirubin in hepatocytes

A

Rotor syndrome

21
Q

Charcots TRIAD

A

Fever
Jaundice
RUQ pain

22
Q

Cholestatis and paucity of bile ducts

A

Alagille syndrome

23
Q

Severe UGT1A1 deficiency

A

Criggler-Naijar Type 1
this involved in conjugation of bilirubin

24
Q

Treatment for Extrahepatic biliary atresia

A

Kasai procedure

25
Associated conditions Primary Biliary Cholangitis
Sjogren syndrome Hashimoto thyroditis Scelroderma female, + AMA histo: Florid duct lesion, elongated cirrhotic nodules nodular regenerative hyperplasia
26
Radiology seen in Primary Sclerosing Cholangitis
Strictures and beading of large bile ducts assoc. IBD + ANCA onion skin strictures
27
Sequelae of PBC
Increase risk of HCC
28
Sequalae of PSC
inc risk of cholangicarcinoma
29
MCC of small portal vein obstruction
Schistomiasis
30
Sinusoidal dilation secondary to impaired efflux of hepatic bloody
Peliosis hepatis
31
liver enlargement, pain and ascites secondary to thrombosis
Budd-Chiari Syndrome
32
MC benign tumor
Cavernous Hemangioma
33
MC liver tumor of early childhood
Hepatoblastoma
34
MC primary malignant tumor
HCC
35
2nd MC Primary malignant tumor
Cholangiocarcinoma
36
Nodules/tumor: obese young women, taking OCP and anabolic steroid angiography: Hypovascular
Hepatocellular adenoma assoc with: OPCa and anabolic steroid Obese, metabolic syndrome
37
Adult women central stellate scar angiography: Hypervascular wtih dense capillary blush
Focal nodular hyperplasia (vascular lesion) liver scan: Normal to inc uptake
38
MC Congenital anomaly of the Gallbladder
folded fundus "Phrygian cap"
39
mucosal cholesterol-laden macrophages
Cholesterolosis radiolucent seen in Cholesterol stone
40
MC biliary tract disease
Cholelithiasis RF: forty, female, fat
41
Calculous Mononuclear cells in GB Rokitansky-Aschoff sinuses
Chronic Cholecystitis notable forms: Porcelain GB - calcification Hyalinazing - fibrosing Xanthogranulomatous cholecystitis Hydrops
42
MC pancreatic anomaly
Pancreatic divisum failure of fusion of fetal pancreatic ducts
43
congenital anomaly cause by mutation of PDX1 mutation
Agenesis of pancreas