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
2
Q
Causes of Chronic Pancreatitis
A
- Adults: alcoholism
- Children: cystic fibrosis
- 25% - idiopathic form
3
Q
- presumed autoimmune causation with characteristic
laboratory, histologic, and morphologic findings - include AIP and idiopathic duct centric pancreatitis (IDCP)
A
AUTOIMMUNE PANCREATITIS
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
5
Q
histologically confirmed, with granulocytic infiltration of the duct wall (GEL), but without lgG4 positive cells and systemic
involvement
A
IDCP
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)
7
Q
Tx for AIP
A
Glucocorticoids: Prednisone
8
Q
Tx for Refractory symptoms. A monoclonal antibody directed against B cells
A
Rituximab
9
Q
imaging initial modality of choice of AIP
A
Abdominal CT
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
11
Q
Tx that improve pain in chronic pancreatitis and lower pain medication requirement
A
Pregabalin
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
13
Q
- embryologic ventral and dorsal pancreatic anlagen fail to fuse
- most common congenital anatomic variant of the human
pancreas
A
PANCREAS DIVISUM