Internal_Disorders of the pancreas Flashcards
(45 cards)
Which enzyme gene mutation causes hereditary pancreatitis?
A) carbonic anhydrase
B) cationic trypsin
C) phospholipase
D) kallikrein
E) hexokinase
B) cationic trypsin
The main functions of pancreatic ductal cells, except:
A) to guarantee a shell for th acinic cells
B) to excrete a liquid rich in bicarbonate
C) to bring the enzymes produced by the acini into the duodenum
D) to neutralize the protons produced by acini through bicarbonate secretion
E) to excrete a liquid rich in sodium and chloride ions
E) to excrete a liquid rich in sodium and chloride ions
It is true for the enzymes produced by pancreas:
A) Three different enzymes are produced by acini: amylase, trypsin and lipase
B) The enzymes are activated under physiological conditions in the pancreatic duct.
C) Lipase is activated by the enzyme enterokinase in the duodenum.
D) Enzymes are produced in inactive state in acini and under physiological conditions they only become activ in duodenum.
E) Most of the enzymes are produced by pancreatic ductal cells.
D) Enzymes are produced in inactive state in acini and under physiological conditions they only become activ in duodenum.
It is true for acute pancreatitis, except:
A) Antibiotic therapy should always be used due to the risk of infection.
B) The lipase level increases in the blood.
C) Usually it is induced by gallstone or excessive alcohol consumption.
D) It leads to abdominal pain.
E) The amylase level increases in the blood.
F) The inflammation can also spread to other organs in severe cases.
A) Antibiotic therapy should always be used due to the risk of infection.
It is characteristic for the SPINK1 gene:
A) It is located on chromosome 8.
B) It encodes a protein called pancreatic secretory trypsin inhibitor.
C) The production of the protein that it encodes is essential for the activation of trypsin.
D) Its mutation leads in all cases to pancreatitis.
E) It often occurs in pancreatitis with hereditary or familial accumulation.
B) It encodes a protein called pancreatic secretory trypsin inhibitor.
12 In case of cystic fibrosis, the most endangering for the patient’s life is:
A) pancreatic insufficiency
B) gallstones
C) colonic stricture
D) pulmonary complications
E) meconium ileus
F) complications of diabetes mellitus
G) biliary cirrhosis
D) pulmonary complications
In case of acute pancreatitis, the first thing to do is:
A) performing a CT scan
B) performing an ERCP test
C) starting fluid replacement
D) surgical console
E) performing an MRCP test
C) starting fluid replacement
It is true for the distant complications of acute pancreatitis, except:
A) Lungs, kidneys and liver are the most common affected.
B) They are not related to the severity of the disease.
C) Migratory leukocytes, cytokines and free radicals are primarily responsible for their development.
D) The inflammation of organs may also lead to dysfunction and may cause multiple organ failure (MOF).
E) In severe cases, intensive therapy may be also needed.
B) They are not related to the severity of the disease.
It refer to the severity of the acute necrotizing pancreatitits, except:
A) Ranson’s prognostic criteria
B) Glasgow prognostic criteria
C) Apache II. prognostic criteria
D) amylase elevation
E) markers of the inflammatory reaction (TNF-α, IL-6, CRP etc.)
F) CT findings (Balthazar-score) with contrast agent enhancement
G) clinical picture
H) infected necrosis
D) amylase elevation
The most sensitive and specific imaging method is for the diagnosis of chronic pancreatitis:
A) transabdominal ultrasound
B) abdominal CT
C) endoscopic ultrasound
D) ERCP
E) native abdominal X-ray
F) irrigoscopy
D) ERCP
In the case of chronic pseudocysts, primarily selectable procedures are, excluded:
A) percutaneous drainage
B) endoscopic cystogastrostomy or cystoduodenostomy
C) transpapillar drainage of the pseudocyst
D) surgical cystogastrostomy posterior or cystoduodenostomy
E) surgical cystowirsungogastrostomy or cystowirsungo-jejunostomy
A) percutaneous drainage
Mutations in the CFTR molecule in the pancreas can cause the following diseases or increase their risks, except:
A) cystic fibrosis
B) chronic pancreatitis
C) acute pancreatitis
D) pancreatic carcinoma
E) pancreatic division
E) pancreatic division
It is valid for the endoscopic retrograde cholangiopancreatography (ERCP):
1) It is an unlimited repeatable, uncomplicated procedure.
2) The obstruction of the choledochus and the pancreas line can be solved by an additional intervention.
3) It is always diagnostic in mild chronic pancreatitis as well.
4) It has a high sensitivity and specificity in case of pancreatic head tumors.
A) the 1., 2. and 3. answers are correct
B) the 1. and 3. answers are correct
C) the 2. and 4. answers are correct
D) only the 4. answer is correct
E) all of the answers are correct
C) the 2. and 4. answers are correct
2) The obstruction of the choledochus and the pancreas line can be solved by an additional intervention.
4) It has a high sensitivity and specificity in case of pancreatic head tumors.
14 It is characteristic of cystic fibrosis:
1) CFTR gene mutations with autosomal recessive inheritance cause cystic fibrosis disease
2) CFTR protein is a cationic channel located on pancreatic acinic cells
3) mutations reduce the amount or inhibit the function of CFTR protein
4) Cystic fibrosis is the rarest anomaly with recessive inheritance in the Caucasian population
A) the 1., 2. and 3. answers are correct
B) the 1. and 3. answers are correct
C) the 2. and 4. answers are correct
D) only the 4. answer is correct
E) all of the answers are correct
B) the 1. and 3. answers are correct
1) CFTR gene mutations with autosomal recessive inheritance cause cystic fibrosis disease
3) mutations reduce the amount or inhibit the function of CFTR protein
It is valid for transabdominal pancreatic ultrasound diagnostics:
1) unlimited repeatable, relatively cheap
2) suitable for detecting fluid collections and pseudocysts
3) meteorism is not an obstacle
4) the accompanying bile disease can be well proven
5) edema is well separated from necrosis
6) obesity is not an obstacle
7) ductal diatation can be well recognized
A) the 1., 2. and 3. answers are correct
B) the 4., 5., 6. and 7. answers are correct
C) the 1., 2., 3. and 4. answers are correct
D) the 1., 2., 4. and 7. answers are correct
E) all of the answers are correct
D) the 1., 2., 4. and 7. answers are correct
1) unlimited repeatable, relatively cheap
2) suitable for detecting fluid collections and pseudocysts
4) the accompanying bile disease can be well proven
7) ductal diatation can be well recognized
It is valid for pancreatic computer tomography (CT):
1) unlimited repeatable, relatively cheap
2) suitable for detecting fluid collections and pseudocysts
3) obesity and meteorism are not obstacles
4) it also detects small parapapillary tumors
5) edema is well separated from necrosis
6) calcification and ductal diatation can be well recognized
A) the 1., 2., 3. and 6. answers are correct
B) the 3., 4. and 5. answers are correct
C) the 2., 3., 5. and 6. answers are correct
D) all of the answers are correct
C) the 2., 3., 5. and 6. answers are correct
2) suitable for detecting fluid collections and pseudocysts
3) obesity and meteorism are not obstacles
5) edema is well separated from necrosis
6) calcification and ductal diatation can be well recognized
It is characteristic of pancreatic tumors:
1) the five-year survival rate is below 5%
2) it usually begins with jaundice and severe spastic abdominal pain
3) it mainly origins from acinic cells
4) it never causes pancreatitis
5) it responds well to cytostatics
A) the 1., 2. and 3. answers are correct
B) the 1., 2. and 4. answers are correct
C) the 1., 2. and 5. answers are correct
D) only the 1. answer is correct
E) the 3. and 4. answers are correct
D) only the 1. answer is correct
1) the five-year survival rate is below 5%
Pair them.
I can heal Restitutio ad integrum, plenty of fluid replacement, gallstone.
A) acute pancreatitis
B) chronic pancreatitis
C) pancreatic tumor
D) cystic fibrosis
A) acute pancreatitis
Pair them.
Weight loss, painless icterus
A) acute pancreatitis
B) chronic pancreatitis
C) pancreatic tumor
D) cystic fibrosis
C) pancreatic tumor
Pair them.
Alcohol, fatty stool discharge, maldigestion
A) acute pancreatitis
B) chronic pancreatitis
C) pancreatic tumor
D) cystic fibrosis
B) chronic pancreatitis
Pair them!
Apical Cl- channel, thickening of the glandular secretion, ∆F508-mutation
A) cationic trypsin (PRSS1)
B) chymotrypsin C (CTRC)
C) cystic fibrosis transregulator (CFTR)
D) pancreatic secretory trypsin inhibitor (SPINK1)
C) cystic fibrosis transregulator (CFTR)
Pair them.
Autosomal recessive inheritance, involvement of the lung
A) acute pancreatitis
B) chronic pancreatitis
C) pancreatic tumor
D) cystic fibrosis
D) cystic fibrosis
Pair them!
Recurrent acute pancreatitis attacks, hereditary pancreatitis, 40-50x risk for the developement of pancreatic carcinoma, p.R122H-mutation.
A) cationic trypsin (PRSS1)
B) chymotrypsin C (CTRC)
C) cystic fibrosis transregulator (CFTR)
D) pancreatic secretory trypsin inhibitor (SPINK1)
A) cationic trypsin (PRSS1)
Pair them!
p.N34S mutation, mainly idiopathic pancreatitis.
A) cationic trypsin (PRSS1)
B) chymotrypsin C (CTRC)
C) cystic fibrosis transregulator (CFTR)
D) pancreatic secretory trypsin inhibitor (SPINK1)
D) pancreatic secretory trypsin inhibitor (SPINK1)