Pancreatic Histopath Flashcards

1
Q

Role of the pancreas

A

Production of 2L a day of enzymic HCO3 rich fluid, stimulated by secretin & CCK

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2
Q

Role of secretin (2) & produced by which cells

A

Produced by s-cells of duodenum - in response to acid chyme from stomach Stimulates HCO3- release from pancreas (centroacinar cells)

Inhibits gastric acid secretion from parietal cells

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3
Q

Role of CCK (2) & produced by which cells

A

Produced by I-cells of duodenum (in response to food in duodenum)

Stimulates digestion of fat & protein by causing release of digestive enzymes (from acinar cells)

Stimulates gallbladder contraction > release bile

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4
Q

Function of alpha cells, beta cells, delta cells,

A

alpha - glucagon beta - insulin delta - somatostatin (endocrine cyanide)

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5
Q

Function of D1 cells &

pancretic polypeptide cells

A

D1 cells - a vasoactive intestinal peptide (VIP) that stimulates secretion of H2O

PP cells - secrete PP, which stimulates secretion of gastric & intestinal enzymes, whilst reducing intestinal motility. Self regulates secretion activities

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6
Q

Criteria of metabolic syndrome (5)

A

Dyslipidaemia - HDL 2mmol/l

Fasting blood sugar > 6mmol/l

BP > 140/90

Central obesity > 94 cm in M, > 80 cm in F

Microalbuminaemia

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7
Q

Diagnosis of DM

A

fasting plasma glucose > 7 mmol/l

Random blood glucose > 11.1 mmol/l

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8
Q

Symptoms of DM (3)

A

Polyuria

Polydipsia

Recurrent infections

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9
Q

Macrovascular complications of diabetes (3)

A

Cardiac - MI

REnal - GN or pyelonephritis

Cerebral - CVA

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10
Q

Microvascular complications of diabetes (2)

A

Ocular - diabetic retinopathy

PVS - claudication,

poor healing ulcer

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11
Q

Causes of Acute pancreatitis (11)

A

I - idiopathic, G - gallstones, E - ETOH, T - trauma, S- steroids, M - mumps, A - autoimmune, S - scorpion venom, H - Hyperlipidaemia, E - ERCP, D - Drugs e.g. thiazides

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12
Q

Presentation of acute pancreatitis (3)

A

Severe epigastric pain - relieved by leaning forward

Vomiting Pain radiates to back

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13
Q

Histology of acute pancreatitis (1)

A

Coagulative necrosis

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14
Q

Complication of acute pancreatitis (1)

A

formation of pseudocyst

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15
Q

Ix of acute pancreatitis (1)

A

serum LIPASE (amylase on transiently increased)

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16
Q

Causes of chronic pancreatitis (5)

A

Alcoholism

Pancreatic duct obstruction e.g. stone

Autoimmune

CF

Hereditary

17
Q

Presentation of chronic pancreatitis (3)

A

epigastric pain radiating to back

Malabsorption results in weight loss & steatorrhea secondary DM - due to lack of enzymes to digest food

18
Q

Histology of chronic pancreatitis (3)

A

Fibrosis + loss of exocrine tissue

Duct dilatation with thick secretions

calcification

19
Q

Acinar cell carcinoma presentation (4)

A

A rare cancer seen in eldery,

get enzyme secretion by neoplastic cells

Presentation - non specific weight loss, abdo pain, nause & vomiting

10% get multi-focal fat necrosis & polyarthralgia - due to lipase

20
Q

Histolopath of acinar cell carcinoma (3)

A

neoplastic epithelial cells with eosinophilic granular cytoplasm positive immunoreactivity for lipase, trypsin, chymotrypsin

21
Q

Prognosis of acinar cell carcinoma

A

Poor - median survival 18 months, 5 yr

22
Q

Ductal adenocarcionma of pancreas epidemiology - age group, gender & site

A

85% of all pancreatic cancers

Age > 60

M> F

Head of pancreas - Causes obstruction of bile duct > jaundice

23
Q

Ductal adenocarcionma of pancreas risk factors (3)

A

Smoking

diet

Genetic e.g. HNPCC & FAP

24
Q

Clinical features of Ductal adenocarcionma of pancreas (8)

A

Cachexia & anorexia

Epigastric + back pain - chronic & severe

Jaundice (PAINLESS), pruritis, steatorrhea

Ascites

Abdo mass

Virchow’s node

Trousseau’s syndrome (25%) - recurrent superficial thrombophlebitis

Courvoisier’s sign

25
Q

Investigations of Ductal adenocarcionma of pancreas (3)

A

Bloods - low Hb, high Br, high Ca2+

CT/MRI/ERCP

CA19.9 > 701 (low spec & sens - only used after diagnosis established)

26
Q

Management of Ductal adenocarcionma of pancreas (3)

A

Chemo is palliative 5-FU

Surgery - Whipple’s procedure

Poor prognosis - 5 yr survival

27
Q

Where are neuroendocrine tumours usually found? (2)

A

Body or tail of pancreas

28
Q

neuroendocrine tumours lie on a spectrum (benign > malignant) can be functional give examples (3)

A

Insulinoma - _hypoglycaemic attack_s

Gastrinoma - Zollinger-Ellison syndrome - recurrent ulceration due to high acid output

Glucagonoma - Necrolytic migrating erythema

VIPoma - diarrhoea

29
Q

Non functional neuroendocrine tumours

A

incidental finding on imaging or when large enough to produce symptoms

30
Q

Ix & Rx of neuroendocrine tumours

A

CT/ MRI

Surgery

31
Q

MEN-1 (3)

A

PPP

Pancreatic endocrine tumour (often a phaeo)

Parathyroid

Pituitary adenoma

32
Q

MEN 2A (3)

A

Parathyroid

Thyroid

Phaeo

33
Q

MEN 2B (3)

A

Medullary thyroid

Phaeo

Neuroma MARFINOID PHENOTYPE

34
Q

Pancreatic malformations (3)

A

Ectopic pancreas - esp stomach/ small intestine

Pancreas divisum - failure of fusion of dorsal + ventral buds; increased risk of pancreatitis

Annular pancreas - can present with duodenal obstruction (1 yr)