Path 17-18 GI and Liver Flashcards

1
Q

Duodenal atresia cause

A

Failure to recanalize

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2
Q

Duodenal atresia sx

A

Bilious vomit and abd distension

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3
Q

Pyloric stenosis presentation

A

Palapable mass, nonbilious vomit at 2-6 weeks

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4
Q

Eosiniphilic esophagitis cause

A

Food allergens

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5
Q

Plummer vinson syndrome

A

DIES

Dysphagia, iron deficiency, esophageal webs, squamous cell carcinoma

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6
Q

Barret esophagus caused by

A

GERG

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7
Q

Barret esophagus pathology

A

Intestinal metaplasia replaces squamous epithelium

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8
Q

Esophageal cancer: portions affected

A

Squamous: Top 2/3
Adenocarcinoma: Bottom 1/3

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9
Q

NSAID gastritis how

A

decreased PGE2 means leads to lower gastric mucosa protection

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10
Q

Cushing ulcer pathogenesis

A

Vagal stim —> ACh increases —> H+ increases

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11
Q

Autoimmune gastritis caused by

A

Autoantibodies to H+/K+ ATPase on parietal cells

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12
Q

H pylori vs autoimmune gastritis location

A

H pylori antrum

Autoimmune body and fundus

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13
Q

Menetier disease pathology

A

Hyperplasia of gastric mucosa make rugae

Decreased acid production

Edema and other GI sx

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14
Q

Gastric adenocarcinoma outward signs

A

Virchow node, sister mary joseph node

Acanthosis nigricans

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15
Q

Celiac disease findings

A

IgA antitissue transglutaminase

Crypt hyperplasia

Gliadin peptide antibodies

Villious atrophy

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16
Q

Tropical sprue caused by

A

Infection. Infectious celiac. Pathogen unk

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17
Q

Whipple disease cause

A

Tropheryma whilpplei cause

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18
Q

Whipple disease histo and sx

A

PAS+ foamy macrophages

Cardiac, Arthralgia, Neuro sx

PAS FOAMY WHIPPED CAN

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19
Q

Chrons location

A

Ususally colon, spares rectum

Skip lesions

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20
Q

Ulcerative colitis location

A

Whole colon, continous

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21
Q

Chrons morphology

A

Fistulas, cobblestone mucosa, string sign on barium swallow, linear fissures

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22
Q

Chron disease histo

A

Non caseating granulomas and lymphoid aggregates

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23
Q

Ulcerative colitis location

A

Only affects mucosa and submucosa

LEAD PIPE appearance (no haustra)

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24
Q

Ulcerative colitis histo

A

Crypt absecess and bleeding

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25
Chrons vs UC disease mediated by
Chrons Th1 UC Th2
26
UC vs Chrons: bloody diahreah?
UC: bloody Chrons: sometimes bloody
27
Ulcerative colitis associated antibodies
p-ANCA
28
Toxic megacolon seen with (chrons/UC)
Ulcerative colitis
29
McBurney point location
1/3 distance from ASIS to ubilicus
30
Diverticulosis pathology
MAny false diverticula in colon
31
Diverticulitis presentation
LLQ pain, fever, leukocytosis
32
Meckel vs false diverticulum
Meckel: all layers False: only mucosa and submucosa
33
Zenker diverticulum pathology
False diverticulum at Killian triangle
34
Hirshprung dx pathogenesis
Congenital lack of nervous plexus in distal colon leads to toxic megacolon
35
Hirschprung disease embryo cause
Failure of neural crest cell migration
36
Hirschprung disease gene abnormality
RET
37
Volvulus xray appreance
Coffee been sign
38
Intussuseption sx
PAin, bloody red jelly stool
39
Most common small bowel obstruction
Adhesion s/p surgery
40
Hamartoma polyps associated with
Peutz-Jeghers syndrome
41
Adenomatous polyp histo
Tubular or Villous Villous more cancerous
42
Adenomatous polyps gene
APC KRAS
43
Familial denomaptous polyposis gene
Autosomal domminant APC tumor suppression gene
44
Gardner syndrome
FAP (familial polyposis) + soft tissue or bone tumor
45
Turcot syndrome
FAP (famililal polyposis) + neural tumors
46
Colon cancer presentation
Iron deficiency anemia in elderly, IBD, apple core xray, weight loss
47
Colorectal cancer tumor marker
CEA
48
Smoking protective for
Ulcerative colitis
49
Colon cancer gene mutation
APC —> KRAS —>TP53 AK 53
50
Cirrhosis cell type
Stellate cells
51
Cirrhosis histo
Difuse fibrosing by stellate cells, regenerative nodules
52
Primary bacterial peritonitis sx
ASCITES Sepsis, ileus, diagnosed by high neutrophils in ascitic fluid
53
In alcoholic live which transferase is elevated more
AST > ALT
54
Alk phos goes up in _____
Bone disease and **cholestasis**
55
Reye syndrome MOA
Aspirin metabolites decrease β oxidation by inhibiting mitochondria. Fucks up liver
56
Reye syndrome sx
SHINE Steatosis of liver Hypoglycemia Infection Not alert Encephalopathy
57
Hepatic steatosis
Macrovesicular fatty change reversible
58
Alcoholic hepatitis histo
Swollen and necrotic hepatocytes with neutrophil inflammation **Mallory bodies**
59
Nonalcaholic fatty liver dx moa
Insulin resistance leads fatty infiltration of hepatocytes
60
Most common primary malignancy of liver
Hepatocellular carcinoma
61
Virus that causes hepatocellular cancer
HBV
62
Hepatocellular carcinoma clinical features
Jaundice, ascites, hepatomegaly **polycethemia**
63
Hepatocellular carcinoma labs
elevated α-fetoprotein
64
Angiosarcoma of liver is from what exposure
Arsenic, vinyl chlorida
65
Most common benign liver tumor
Cavernous hemangioma
66
Budd chiari syndrome pathology
Thrombosis/compression of hepatic vein causes congestive liver sx.
67
Causes of jaundice
HOT Liver Hemolysis Obstruction Tumor Liver dx
68
α1- anti trypsin pathogenesis liver
Misfolder gene product with protein aggregates in hepatocellular ER
69
α1- antitrypsin liver progression
Causes PAS+ cirrhosis
70
Conjugated hyperbillirubinemia causes
Biliary obstruction Dubin Johnson Rotor syndrom
71
Unconjugated hyperbilirubiemia caused by
Hemolytic anemia , gilbert syndrome, Crigler-najjar
72
Pysiologic neonatal jaundice caused by
immature UDP-glucuronosyltransferase
73
Billiary atresia presentation
Jaundice 2 weeks after birth, dark urine, acholic stool Elevated direct bilirubin and GGT
74
Biliary atresia pathogenesis
Fibro-obliterative destruction of extra hepatic bile ducts
75
Heriditary hyperbilirubenimias genetics
autosomal recessive
76
Gilber syndrome pathogenesis
decreased UPD-glucoronosyltransferase activity
77
Gilbert syndrome presentations
Assymptomatic jaundice after stress
78
Crigler Najjar syndrome pathogenesis
UPD-glucoronosyltransferase leads to no conjugation
79
Crigler-Najjar findings
Jaundice, kernicters, increased indirect bilirubin
80
Dubin johnson pathogenesis and findings
Conjugated hyperbili from defective liver excretion Black liver
81
Wilson disease gene mutation and chromosome
13 ATP7B gene
82
Wilson disease pathogenesis
Copper transport ATPase means copper cant be excreted into bile. Copper accumulates and is found in urine
83
Wilson disease findings
Low ceruloplasmin Eye rings, neuropsych issues, renal dx (fanconi)
84
Wilson dx treatment
Copper chelation with penicillamine and oral zinc
85
Hemochromatosis genetics
autosomal recessive HFE gene chromosome 6
86
Hemochromatosis pathogenesis
Abnormal iron sensing leads to increased intestinal absorption Iron overload
87
Hemochromatosis labs
Elevated: ferritin, iron, transferin Decreased: TIBC
88
Hemocrhomatosis presentation
Cirrhosis, diabetes, bronze skin
89
Hemochromatosis cardiac complication
Restrictive cardiomyopathy
90
Biliary tract disease presentation
Pruritus, jaundice, dark urine, light colored stool
91
Cholestatic pattern (lab values)
Increased: Conjugated bilirubin, cholesterol, AlkPhos, GGT
92
Primary sclerosing cholangitis pathology
Onion skin bile duct fibrosis
93
Primary sclerosin cholangitis patient population
Middle aged men w/ UC
94
Primary sclerosing colangitis associated conditions and labs
Ulcerative colitis (p-anca) Increased IgM Can lead to cholangiocarcinoma and gall cancer
95
Primary biliary cholangitis pathology
Autoimumine reaction Lymphocytic infiltrate with destruction of lobular bile ducts
96
Primary biliary cholangitis seen (population)
Middle age woman
97
Primary biliary cholangitis additional findings
Anti-mitochondichondrial antibodies Increased IGM Associated with autoimmune conditions
98
Risk factors for gall stones
4 Fs Fat female fertile forty
99
Cholesterol stones feautues
Yellow Radiolucent
100
Cholesterol stones seen in
Chrons dx, elderly
101
Bilirubin stone features
Black Radiopaque
102
Infectious stone features
Brown, radiopaque
103
Gall stone causes
Increased cholesterol or bilirubin Decreased bile salts Gallbladder stasis
104
Biliary colic caused by
Neurohormonal activation
105
Cholecystitis causes
Calculous: stones Acaclulous: gallbladder stasis, shock
106
Gallstone ileus
Gallbladder/GI tract fistula leads to stone entering lumen and obstructing ileocecal valve
107
Porcelain gall bladdercaused by
Chronic cholecystitis
108
Porcelain gallbladder increases risk of
Gallbladder adenocarcinoma
109
Ascending cholangitis findings
Really fucking sick Fever, RUQ, jaundice plus shock and AMS