60 - Pancreatic Pathology Flashcards

1
Q

Exocrine function of pancreas

A

85% of pancreatic tissue
secrete digestive enzymes: trypsin, lipase, phospholipase, elastase, amylase, which are markers for pancreatic inflammation and require activation

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2
Q

Endocrine function of pancreas

A

Islets of Langerhans

Secrete peptide hormones into blood (e.g. insulin and glucagon)

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3
Q

Acute pancreatitis - clinical presentation

A

Usually emergency
Sudden onset of severe abdo pain radiating to back
Nausea and vomiting
May be mild (recover within 5-7days) but has a high mortality as well

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4
Q

Acute pancreatitis - investigations

A

Raised serum amylase/lipase (3x normal)

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5
Q

Acute pancreatitis - aetiology

A

Gallstones (50%)
Alcohol (25%)
Rare causes: vascular insufficiency, viral infections (mumps, Coxsackie B), hypercalcaemia, ERCP
Idiopathic (10%)

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6
Q

Acute pancreatitis - pathogenesis

A

Leakage and activation of pancreatic enzymes

Amylase into blood

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7
Q

Acute pancreatitis - mild

A

Swollen gland with fat necrosis

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8
Q

Acute pancreatitis - severe

A

Swollen, necrotic gland with fat necrosis and haemorrhage

Showing Grey Turner’s sign and Cullen’s sign

Hypocalcaemia (fatty acids bind calcium ions), hyperglycaemia, abscess formation, pseudocysts

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9
Q

Acute pancreatitis - Grey Turner’s sign

A

Haemorrhage into sub cut tissues of flank

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10
Q

Acute pancreatitis - Cullen’s sign

A

Haemorrhage into sub cut tissues of periumbilicus

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11
Q

Acute pancreatitis - complications

A

Shock
Intravascular coagulopathy
Haemorrhage
Pseudocysts (collections of pancreatic juice secondary to duct rupture)

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12
Q

Chronic pancreatitis -

A

Progressive inflammatory disorder in which parenchyma of pancreas is destroyed and replaced by fibrous tissue.

Irreversible dmg to exocrine then to endocrine

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13
Q

Chronic pancreatitis - clinical presentation

A

malnutrition and diabetes

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14
Q

Chronic pancreatitis - causes

A

Toxic - -OH, smoking, drugs, hypercalcaemia, HPTism, infections
Genetic CFTR, PRSS1, SPINK1 mutation
Obstruction of main duct - cancer, scarring
Recurrent acute
Autoimmune
Idiopathic

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15
Q

Chronic pancreatitis - main causes

A

95% are alcohol or idiopathic

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16
Q

Chronic pancreatitis - complications

A

Malabsorption of fat (lack of lipases) - steatorrhoea, impairment of fat soluble vit absorption (A,D,E,K), diarrhoea, weight loss and cachexia

Diabetes (last feature)
Pseudocysts
Stenosis of common bile duct / duodenum

17
Q

Chronic pancreatitis - mortality

A

nearly 50% within 20-25 yrs of onset

18
Q

Pancreatic adenocarcinoma -

A

Most common type - 90% of pancreatic neoplasms

4% 5 yr survival rate

19
Q

Pancreatic adenocarcinoma - who?

A
60-80 yrs (rare before 40)
1.3M:1F
Smoking (2-3x risk), drops with abstinence
Heavy alcohol
Red meats
Obesity
Hereditary (10%)
Chronic pancreatitis
20
Q

Pancreatic adenocarcinoma - clinical presentation

A
Present for at least a decade before detected
Non-specific symptoms
Epigastric pain, radiating to back
Weight loss, painless jaundice, pruritis and nausea
Trousseau's syndrome
Courvoisier's sign
Distant mets (liver, peritoneum, lung)
Diabetes
21
Q

Pancreatic adenocarcinoma - Trousseau’s sign

A

Migratory thrombophlebitis

22
Q

Pancreatic adenocarcinoma - Courvoisier’s sign

A

Palpable gall bladder w/o pain

23
Q

Pancreatic adenocarcinoma - poor prognosis factors

A

Extension of tumour outside pancreas
Met spread to local lymph nodes
Vascular and perineural invasion
Grade of differentiation

24
Q

Pancreatic neuroendocrine tumours -

A

Uncommon

25
Q

Pancreatic neuroendocrine tumours - clinical presentation

A

Autopsy studies- higher incidence (up to 10%)
20-60 yrs
M=F
Increased risk MEN 1, von Hippel Lindau