Chronic Pancreatitis Flashcards

1
Q
  • is a disease process characterized by irreversible damage to
    the pancreas
  • stellate cell activation that results in cytokine expression and production of extracellular matrix proteins cause acute and chronic inflammation and collagen deposition in the pancreas
  • defined by the presence of histologic abnormalities, including chronic inflammation, fibrosis, and progressive destruction of both exocrine and eventually endocrine tissue atrophy
A

CHRONIC PANCREATITIS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Causes of Chronic Pancreatitis

A
  • Adults: alcoholism
  • Children: cystic fibrosis
  • 25% - idiopathic form
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q
  • presumed autoimmune causation with characteristic
    laboratory, histologic, and morphologic findings
  • include AIP and idiopathic duct centric pancreatitis (IDCP)
A

AUTOIMMUNE PANCREATITIS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q
  • the pancreas is involved as part of an lgG4 systemic disease and meets HISORt criteria
  • pancreatic histopathologic findings include lymphoplasmacytic infiltrate, storiform fibrosis, and abundant IgG4 cells
A

AIP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

histologically confirmed, with granulocytic infiltration of the duct wall (GEL), but without lgG4 positive cells and systemic
involvement

A

IDCP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q
  • Mild symptoms, usually abdominal pain, but without frequent attacks of acute pancreatitis
  • Diffuse swelling and enlargement of the pancreas
  • Two-thirds of patients present with either obstructive jaundice or a “mass” in the head of the pancreas mimicking carcinoma
  • Diffuse irregular narrowing of the pancreatic duct (MRCP or ERCP)
  • Increased levels of serum gamma globulins, especially!gG64
  • Presence of other autoantibodies (ANA), rheumatoid factor (RF)
  • Can occur with other autoimmune diseases: Sjégren’s syndrome, primary sclerosing cholangitis, ulcerative colitis, rheumatoid arthritis
  • Extrapancreatic bile duct changes such as stricture of the common bile duct and Intrahepatic ducts
  • Pancreatic calcifications (rare)
  • Pancreatic biopsies reveal extensive fibrosis and lymphoplasmacytic infiltration
  • Glucocorticoids are effective in alleviating symptoms, decreasing size of the pancreas, and reversing histopathologic changes
A

Autoimmune Pancreatitis (AIP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Tx for AIP

A

Glucocorticoids: Prednisone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Tx for Refractory symptoms. A monoclonal antibody directed against B cells

A

Rituximab

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

imaging initial modality of choice of AIP

A

Abdominal CT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q
  • diagnostic test with the best sensitivity and specificity
  • hormone stimulation test
  • abnormal when 260% of the pancreatic exocrine function
    has been lost
A

Secretin test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Tx that improve pain in chronic pancreatitis and lower pain medication requirement

A

Pregabalin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  • ventral pancreatic anlage fails to migrate correctly to make
    contact with the dorsal anlage
  • cause intestinal obstruction in the neonate or the adult
  • Symptoms of postprandial fullness, epigastric pain, nausea,
    and vomiting
  • Retrocolic duodenojejeunostomy
A

ANNULAR PANCREAS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q
  • embryologic ventral and dorsal pancreatic anlagen fail to fuse
  • most common congenital anatomic variant of the human
    pancreas
A

PANCREAS DIVISUM

How well did you know this?
1
Not at all
2
3
4
5
Perfectly