Pancreas (for PBR 2) Flashcards
(42 cards)
Two morphologic types of pancreatitis
Interstitial edematous
Acute necrotizing pancreatitis
Imaging finding of interstitial edematous pancreatitis
CE CT:
Localized or diffuse enlargement of the pancreas with normal homogeneous parenchymal
Slightly heterogeneous enhancement due to edema
Mild fat stranding and peripancreatic inflammatory changes may be present with varying fluid volumes of peripancreatic fluid
Acute necrotizing pancreatitis is divided into three forms by CT appearance
- Pancreatic parenchymal necrosis with peripancreatic necrosis
- Peripancreatic necrosis alone
- Pancreatic parenchymal necrosis alone
Most common form of acute necrotizing pancreatitis
Pancreatic parenchymal necrosis with peripancreatic necrosis
Imaging finding of pancreatic parenchymal necrosis with peripancreatic necrosis
Lack of parenchymal enhancement associated with nonliquefied heterogeneous areas of nonenhancement in peripancreatic tissues, most commonly in the lesser sac and retroperitoneum
Pancreatic necrosis is best determined by CT at approximately how many hours following onset of symptoms?
72 hours
Collections associated with interstitial pancreatitis
Initial 4 weeks as nonencapsulated, nonenhancing, low attenuation, liquid collections without solid components
Walls are imperceptible
Acute peripancreatic fluid collections
These are defined as simple collections with perceptible walls seen after 4 weeks
Pseudocyst
Collections associated with necrotizing pancreatitis seen in the first 4 weeks
Acute necrotizing collections
Heterogeneous collections containing hemorrhage, fat, or necrotic fat within or surrounding necrotic pancreatic parenchyma
An enhancing wall may develop around an acute necrotic collection and seen after 4 weeks -
What is the term of the collection?
Walled-off necrosis
WONs appear heterogeneous in attenuation and complex because of variable necrotic tissues and debris
This is caused by recurrent and prolonged bouts of acute pancreatitis that cause parenchymal atrophy and progressive fibrosis
Chronic pancreatitis
Both exocrine and endocrine function of the pancreas may be impaired
Most common cause of chronic pancreatitis
Alcohol abuse (70%)
Biliary stone disease (20%)
Morphologic changes and imaging findings of chronic pancreatitis
- Dilation of the pancreatic duct (usually in a beaded pattern of alternating areas of dilation and constriction)
- Decrease in visible pancreatic tissue because of atrophy
- Calcifications (finely stippled to coarse)
- Focal-mass-like enlargement of the pancreas (owing to benign inflammation and fibrosis)
- Stricture of the bile duct (because of fibrosis or mass in the pancreatic head resulting in proximal bile duct dilation)
- Fascial thickening and chronic inflammatory changes in surrounding tissues
Also known as lymphoplasmacytic sclerosing pancreatitis
Unique form of pancreatitis caused by autoimmune disease associated with elevation of IgG4
Autoimmune pancreatitis
Extrapancreatic manifestations of autoimmune pancreatitis
Inflammatory bowel disease (ulcerative colitis)
Long segment bile duct strictures
Lung nodules
Lymphadenopathy
Lymphocytic infiltrates in the liver and kidneys
Retroperitoneal fibrosis
Sjogren syndrome
Findings that favor diagnosis of autoimmune pancreatitis over adenocarcinoma
- Diffuse or focal swelling of the pancreas with characteristic halo of edema
- Extensive peripancreatic stranding and edema are absent
- Diffuse or segmental narrowing of the pancreatic duct and/or the common bile duct
- Absence of dilation of the pancreatic duct and absence of parenchymal atrophy proximal to the pancreatic mass (theses findings are typically present with adenocarcinima)
- Fluid collections and parenchymal calcifications are typically absent
- Peripancreatic blood vessels are usually not involved
- Kidneys are involved in 1/3 of cases (round-wedge-like , or diffuse peripheral patchy areas of decreased contrast enhancement)
This is an uncommon form of pancreatitis that may also mimic adenocarcinoma
Fibrosis in the groove between the head of the pancreas, the descending duodenum, and the common bile duct produces an inflammatory mass that obstructs the common bile duct
Groove pancreatitis
Characteristic finding of groove pancreatitis
- Sheet-like mass in the pancreaticoduodenal groove
- Atrophy and fibrotic changes in the pancreatic head
- Small cysts along the wall of the duodenum
- Duodenal wall thickening and luminal narrowing
- Tapering stenosis of the common bile and pancreatic ducts
- Widening of the space between the distal ducts and the wall of the duodenum (rarely seen with adenocarcinoma)
- Enhancement is delayed but progressive
Signs of resectability of pancreatic adenocarcinoma
- Isolated pancreatic mass with or without dilation of the bile or pancreatic ducts
- No extrapancreatic disease
- No encasement of celiac axis or SMA
Signs of potential resectability
- Absence of involvement of the celiac axis or SMA
- Occlusion of the superior mesenteric or portal vein without a technical option for reconstruction
- Liver, peritoneal, lung, or any other distant metastases
Evidence of arterial encasement that indicates unresectability
- Tumor abutting >180 degrees of the circumference of the artery
- Tumor abutment focally narrowing the artery
- Occlusion of the artery by tumor
These tumors may be functioning producing hormones resulting in distinct clinical syndromes, or may be nonfunctional and grow to large size before presenting clinically
Neuroendocrine (islet cell) tumors
Different types of neuroendocrine (islet cell) tumors
Insulinomas Gastrinomas Glucagonoma Somatostatinoma VIPoma
80% of nonfunctioning tumors are:
a. benign
b. malignant
Malignant