Data
from our institution demonstrated improved rates of resectability
(ability to remove tumor surgically) when strict, objective CT criteria
are used. These criteria are:
1. the absence of extrapancreatic disease,
2 .a patent superior mesenteric-portal vein confluence, and
3. no direct tumor extension to the celiac axis or superior mesenteric
artery.
Patients whose tumors do not meet these criteria are not considered
candidates for potentially curative surgery.
CT and MR imaging examinations are tailored to the pancreas, rather
than being done as routine screening examinations. We rely on thin-section
CT, preferably with helical scanning done during the early phase
of intravenous contrast enhancement. MR imaging, when done with
fast scanning and fat-suppressed sequences with and without intravenous
contrast enhancement, provides similar information. There has been
no conclusive evidence about which modality is better. The Radiology
Diagnostic Oncology Group, using data obtained from conventional
CT and MR imaging, currently recommends CT for the initial assessment
of patients with pancreatic tumors, but MR imaging can be used when
there is a contraindication (patient allergy) to contrast-enhanced
CT.
Computed Tomography Techniques--specific techniques employed at
M. D. Anderson Cancer Center for CT imaging of the pancreas
Computed Tomography Findings--major radiographic findings with
CT imaging of pancreatic carcinoma
Differential Diagnosis--use of CT to distinguish between types
of pancreatic masses
Vascular Involvement--radiographic assessment of the tumor-blood
vessel relationship
Pathways of Tumor Infiltration--radiographic assessment of tumor
spread
Helical CT Angiography--state-of-the-art assessment of pancreatic
tumors
Endoscopic Retrograde Cholangioapancreatography
(ERCP) and Endoscopic Ultrasound (EUS)
If a low-density mass is not seen on CT scans, despite the presence
of extrahepatic biliary obstruction, patients should undergo ERCP
and EUS. Diagnostic ERCP is used in the setting of extrahepatic
biliary obstruction when CT or EUS fails to identify a neoplastic
cause for biliary obstruction, or when Fine Needle Aspiration (FNA)
under EUS guidance has been nondiagnostic. A malignant obstruction
of the intrapancreatic portion of the common bile duct (CBD) is
characterized by the presence of a stricture in both the intrapancreatic
CBD and the pancreatic duct ("double-duct sign"). This
often can be accurately differentiated from choledocholithiasis,
and the long, smooth tapering stricture seen with chronic pancreatitis.
Tissue diagnosis may be obtained at the time of ERCP. Finally, the
absence of findings consistent with malignancy on ERCP combined
with the absence of a low density mass on high-quality CT makes
periampullary malignancy unlikely. ERCP may also be therapeautic;
endoscopic biliary decompression is necessary in patients with symptoms
of pruritus or cholangitis, and in patients with asymptomatic hyperbilirubinemia
who are to be treated with chemoradition prior to surgery. Plastic
stents (11.5 Fr.) are used in patients with potentially resectable
disease, and expandable metal stents (10 mm) are preferred in patients
with locally advanced (nonsurgical) disease.
EUS-guided FNA is performed in patients with unresectable disease
(locally advanced or metastatic) and in patients with potentially
resectable primary tumors who are candidates for protocol-based
preoperative chemoradiation. EUS allows for real-time identification
of the suspected malignancy at the time of FNA, which may lead to
improved accuracy over CT-guided FNA. EUS-guided FNA is rapidly
becoming the biospy technique of choice in patients who require
cytologic confirmation of pancreatic malignancy. In addition, EUS
can accurately assess the relationship of the primary neoplasm to
adjacent vascular structures.