Pancreatic path Flashcards

1
Q

what are the functions of the pancreas

A

exocrine - convert trypsinogen to trypsin in the duodenum, acing cells - pyramidal shaped epithelia around lumen
secretes trypsin, lipase, elastase, amylase

endocrine - islets of langerhans insulin (b) and glucagon (a)

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2
Q

what is an exocrine test for pancreatic inflammation

A

inert enzyme which require inflammation

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3
Q

describe pancreatitis

A

inflammation with injury to exocrine parenchyma - acute = gland reverts to normal
chronic = irreversible damage

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4
Q

describe hereditary pancreatitis

A

PRSS1 inherited mutation - AD cationic trypsinogen - resistant to cleavage

SPINK1 mutation AR - reduced trypsin inhibitor = auto digestion of the pancreas

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5
Q

describe acute pancreatitis, pathogenesis and complications

A

common - mainly due to gallstones and alcohol (may be viral)
severe abdominal pain, nausea/vomiting
raised serum amylase/lipase
fat necrosis and haemorrhage
hypocalcaemia and hypoxia = shock and DIC

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6
Q

which disease would you see grey tuners signs and cullens sign and what are they

A

grey turner = haemorrhage into the subcutaneous tissue of flank
cullens sign - periumbillicus

acute pancreatitis

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7
Q

describe the main features of chronic pancreatitis

A

progressive inflammation normal cells replaced by fibrous tissue
irreversible destruction of exocrine tissue followed by endocrine tissue = malnutrition and diabetes

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8
Q

what is the aetiology of chronic pancreatitis

A
TIGARO 
Toxic - alcohol, smoking, drugs, ^Ca
Idiopathic 
Genetic: CF, PRSS1 SPINK1
Autoimmune
Recurrent acute pancreatitis 
Obstruction of main duct
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9
Q

what are the complications of chronic pancreatitis

A
malabsorption 
diabetes 
severe chronic pain
stenosis of bile duct  or duodenum 
impairment of ADEK vitamins 
weight loss and diarrhoea
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10
Q

what is the most common type of pancreatic cancer

A

pancreatic adenocarcinoma

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11
Q
what do these disease have mutation in and what are they all associated with
HNPCC
FAMMM
Familial breast cancer 
Ataxia-telangiectics 
Von-Hippe,-Lindau 
Familial pancreatitis 
Peutz jeghers
A
DNA mismatch repair 
p16/cdkn2a
BRCA2
ATM
VHL
catatonic trypsinogen, SPINK1
LKB1/STK11

all associated with pancreatic cancer

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12
Q

describe the progression model of adenocarcinoma in the pancreas

A

MCN - body of pancreas
IPNN - intraductal
PanIN - most common precursor which starts in duct
KRAS mutations occur early = p16 inactivation - lack suppressor gene

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13
Q

what is pancreatic intraepithelial neoplasia and what does it lead to

A
PanIN 
head of pancreas 
invasive and poorly defined
lots of fibroblasts and lymphocytes 
leads to pancreatic carcinoma
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14
Q

which disease would you see trousseaus syndrome, courvoisior signs Sister Mary joesph

A

pancreatic carcinoma
TS - migratory thrombophlebitis
CS - palpable gallbladder without pain

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15
Q

what are non-specific symptoms of pancreatic carcinoma

A

epigastric pain, radiating to back, weight loss and painless jaundice

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16
Q

why does pancreatic cancer have a poor prognosis

A

spread to lymph nodes, vascular and perineurial invasion

17
Q

what are pancreatic neuroendocrine tumours

A

derived from islet cells

benign to malignant

18
Q

what is the WHO classification of pancreatic neuroendocrine tumours

A

well differentiated

poor “ - more common in males

19
Q
what is the cell type syndrome and clinical findings of these cancers 
insulinoma 
glucagonoma
gastrinoma 
somatostainoma 
VIPoma
PP-cell PEN
A

Cell type syndrome Clinical findings
β cell Insulinoma syndrome hypoglycemia
α cell Glucagonoma syndrome Stomatitis, rash, diabetes, weight loss
G cell Zollinger-Ellison Peptic ulcer, diarrhoea
δ cell Somatostatinoma syndrome Diabetes, cholelithiasis, hypochlorhydria
Unknown Verner-Morrison Diarrhoea, hypokalaemia, achlorydria
PP cells None None

20
Q

describe the features of an insulinoma

A

common
produces hypoglycaemia
confusion, coma - cerebral damage