GI Pathology Flashcards

1
Q

CCK produced by?

A

I cells in duodenum causing release of digestive enzymes

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2
Q

How much secretion does pancreas produce per day?

A

2 litres

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3
Q

Alpha cells produce?

A

Glucagon

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4
Q

Insulin produced by?

A

Beta cells

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5
Q

Delta cells produce

A

Somatostatin

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6
Q

Pancreatic polypeptide has what role?

A

Self regulates secretions in pancreas

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7
Q

Criteria for metabolic syndrome?

A
Fasting glucose >6
BP >140/90
Central obesity
Dyslipidaemia
Microalbuminaemia
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8
Q

Diagnosis diabetes:

Fasting glucose?

Random glucose?

A

Fasting > 7.0

Random >11.1 mmol /L

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9
Q

Impaired fasting glucose?

A

Fasting glucose 6.0-6.9

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10
Q

Impaired glucose tolerance?

A

Glucose 7.8-11 after 2hr OGTT

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11
Q

Most common causes of acute pancreatitis?

A

Gallstones

Alcohol

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12
Q

Histology of acute pancreatitis?

A

Coagulative necrosis

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13
Q

What is alcoholic pancreatitis associated with?

A

Formation of pseudocyst (collection of fluid)

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14
Q

Top causes of chronic pancreatitis?

A

Alcohol

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15
Q

Neoplastic epithelial cells with eosinophilia granular cytoplasm?

A

Acinar cell carcinoma

*positive immunoreactivity for lipase, trypsin and chymotrypsin

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16
Q

Most common pancreatitis cancer?

A

Invasive Ductal adenocarcinoma

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17
Q

Most common site of pancreatic Ca?

A

Head of pancreas

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18
Q

Risk factors for pancreatic cancer?

A

Smoking, diet, genetic (FAP/HNPCC)

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19
Q

Features of pancreatic Ca?

A

Courvoisier’s:

PainLESS jaundice and palpable gallbladder

+pruritis
+steatorrhoea
+diabetes

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20
Q

Trousseau’s syndrome?

A

Recurrent superficial thrombophlebitis in pancreatic Ca due to hypercoagulabilty

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21
Q

What cancers more commonly in tail of pancreas?

A

Neuroendocrine (islet cell)

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22
Q

Tumour marker for pancreatic Ca?

A

CA19.9

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23
Q

Zollinger Ellison syndrome?

A

Gastrinoma -> high acid output

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24
Q

Necrolytic migrating erythema?

A

Glucagonoma

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25
Men 1?
PPP Parathyroid hyperplasia Phaeochromocytoma Pituitary adenoma
26
Men 2a?
PPM Parathyroid hyerplasia Phaeochromocytoma Medullary thyroid cancer
27
Men 2b?
PMM Phaeochromocytoma Medullary thyroid cancer Marfanoid
28
Surgery for pancreatic Ca?
Whipples
29
VIPomas cause?
Diarrhoea
30
Hypoglycaemic attacks?
Insulinoma
31
Ectopic pancreas sites?
Stomach, small intestine
32
Failure of fusion of dorsal and ventral buds?
Pancreas divisum
33
Annular pancreas risk?
Duodenal obstruction around age 1
34
In liver lobule which zone is most metabolically active?
Zone 3 - near central hepatic vein
35
Which zone receives most oxygen and nutrients?
Zone 1 (periportal)
36
Most common benign lesion of liver?
Haemangioma
37
Most common malignant liver tumour?
Metastasis
38
Most common primary liver tumour?
HCC
39
Major causes of cirrhosis?
Alcoholic liver disease NAFLD Hep B/Hep C
40
Most common location of cholangiocarcinomas?
Perihilar
41
Cholangio Ca assoc?
PSC and UC
42
Causes of micronodular cirrhosis (<3mm)?
Alcoholic liver disease Haemochromatosis Biliary tract disease
43
Mallory bodies
Alcoholic liver disease
44
Causes of macronodular cirrhosis? (>3mm)
Viral hepatitis Wilsons a1AT deficiency
45
Child Pugh score <7 indicates?
Child Pugh A 45% 5 yr survival
46
Child's Pugh 7-9
Child's Pugh B 20% 5 yr survival
47
Child's Pugh 10+
Child's Pugh C <20% 5 yr survival
48
Most common cause of chronic liver disease in West?
NAFLD
49
Anti Smooth Muscle antibodies for type 1 Anti LKM for type 2?
Autoimmune hepatitis
50
Anti mitochondrial ab
Primary Biliary Cirrhosis *histology: bile duct loss with granulomas
51
ERCP shows beading of bike ducts due to multi focal strictures?
Primary sclerosing cholangitis
52
Inheritance for haemochromatosis?
Autosomal recessive
53
Incidence rate haemochromatosis?
1 in 400 *1 in 10 caucasians is a carrier
54
HFE gene on chromosome?
6
55
Stain used for iron deposits in liver?
Prussian Blue
56
Features of haemochromatosis?
Grey skin 'Bronze' diabetes Hepatomegaly (microbod cirrhosis) Joint pain
57
Investigations for haemochromatosis? Iron? Ferritin? TIBC? Transferrin sat?
High Fe High ferritin Low TIBC High transferrin sat
58
Treatment for haemochromatosis?
Venesection + desferrioxamine
59
Wilson's disease inheritance?
Autosomal recessive
60
Gene in wilsons?
ATP7B on ch 13
61
Stain in wilsons?
Rhodanine stain for copper
62
Features of wilsons?
Liver disease Neuro - Parkinsonism, psychosis Kayser Fleischer rings
63
Alpha 1 antitrypsin deficiency leads to accumulation of a1AT in intracytoplasmic inclusions which stain with?
Periodic acid schiff
64
Secretin produced by?
S cells of duodenum
65
Mucinous hyperplasia in pancreatic ductal system suggests?
Metaplastic change
66
Mutation associated wi h hereditary pancreatitis?
PRSS1
67
Autoimmune pancreatitis demonstrates a raised......?
IgG4
68
Why are pseudocysts not true cysts?
True cysts surrounded by epithelial cells whereas pseudocysts lined by fibrotic tissue