Pancreas 21-25

Pancreas 21-25

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Q21) All are true about ERCP in pancreatitis except

a) Not useful in patient with multiple strictures and stones

b) Ductal stenting associated with changes of c/c pancreatitis in 50%

c) In pts with pancreas divisum minor duct sphincterotomy causes significant pain relief irrespective of size of duct

d) Pain relief with endoscopic intervention occurs irrespective of relief of ductal pressure/ decrease in duct size.


Q 22 Regarding islet cell of pancreas true is

a) Cells in descending order of frequency is B,D,A,F

b) B cells are more common in the periphery of islets

c ) Peri islet acinar cells same as acinar cells else where

d) Portal flow from islet to acinar cell helps to control secretions


Q 23 . All are true regarding enzyme supplementation in chronic pancreatitis except 

a) Lipase to be given 30000U before or after meal

b) H2 blocker is mandatory with enteric coated tablets

c) Main cause of failure is inadequate dosage

d) In cases of failure of enzyme replacement feeding of medium chain Triglycerides are  helpful


Q24. All of the following predisposing syndromes for pancreatic adenocarcinoma are AD except
A. PJS (Peutz Jeghers) 
B. CFTR (Cystic fibrosis) 
C. HNPCC
D. FAMMM



25. CT severity score for pancreatic necrosis of more than 50%
A. 6
B. 7

C. 10
D. 5


A 21) c

c is false

Pancreatic  ductal  obstruction  by  fibrotic  stenoses  and/or  calculi are  the  most  frequent  indications  for  endoscopic  therapy.

Multiple strictures and stones are not amenable for endoscopic therapy and surgery is preferred. ERCP is contraindicated in multiple stones, intrahepatic stones, biliary anomalies and strictures.

Indications  of ERCp in pancreatitis is cholangitis or sepsis. Ductal stenting for prolonged periods have been associated with pancreatitis (Somogyi and Forsmark 1998) 

In pancreas divisum, minor duct sphincterotomy does not cause  causes good pain relief. Published results consistently show less benefit after minor papilla therapy in those with chronic pancreatitis or chronic pain  compared  with  those  with  recurrent  acute  pancreatitis.


22) d

The islets are composed of four cell types: A (alpha), B (beta), D, and F cells. The four cell types are
not evenly distributed within the islets or throughout the pancreas

Order is BADF

B cells are located centrally in islets and not in periphery. A and F cells are in periphery where as D cells are evenly distributed. 

The rich portal microcirculation of the pancreatic islets allows for the endocrine-to-endocrine cell signaling necessary for hormonal regulation. Afferent arterioles enter the islet in an area of discontinuity in the peripheral, non–B cell mantle of cells. The order of islet cellular perfusion and interaction is from the B cell core outward to the mantle, which is further subordered with most D cells downstream or distal to most A cells. This order allows B cells to inhibit A cell secretion and A cells to stimulateD cell secretion.

REf Sabiston page 941


23 ) b

Indications of enzyme supplementation are -

  1. Weight loss, steatorrhea (15g/day ) or both
  2. Dyspepsia, Diarrhoea, bloating, malabsorption of proteins  and carbohydrates
  3. Pain abdomen

Enteric coated microsphere preparations ( these are special tablets that are coated by polymer and remain unaffected  at low gastric ph)  are better  to decrease stool fat excretion than uncoated tablets.  Uncoated tablets are inactivated by gastric enzymes. So with enteric coated tablets, use of H2 antagonists and PPIs is not required.

All other choices are true

Ref Blumgart


24 b

CFTR is Autosomal Recessive

Several hereditary cancer syndromes (e.g., Peutz-Jeghers syndrome, familial atypical mole and multiple melanoma syndrome, hereditary breast and ovarian cancer syndrome) are known to be associated with increased risk of pancreatic cancer

Hereditary syndromes  which cause pancreatic cancer are

Hereditary pancreatitis (PRSS1 and SPINK1 gene mutation) - Autosomal dominant

Peutz-Jeghers syndrome (STK11 gene mutation) - Autosomal dominant

Cystic fbrosis (CFTR gene mutation). - Autosomal Recessive

Familial atypical mole and multiple melanoma syndrome- Autosomal dominant
(CDKN2A gene mutation)

Hereditary breast and ovarian cancer (BRCA2 gene mutation). Autosomal dominant

Lynch syndrome (mismatch repair gene mutations). Autosomal dominant


25) a

a550d13ee84a0a_13G-TAB-Severity Pancreas 21-25

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