CT Pancreas Protocol for Suspected Pancreatic Pathology
For suspected pancreatic pathology, perform a multiphasic CT with intravenous contrast using a dedicated pancreas protocol that includes thin-slice acquisition (≤3mm), a late arterial/pancreatic phase at 40-50 seconds post-contrast injection, and a portal venous phase at 65-70 seconds. 1, 2
Technical Protocol Specifications
Contrast Administration
- Use non-ionic iodinated contrast agent at 1.5 mL/kg body weight 2, 3
- Injection rate: 4-5 mL/sec for optimal pancreatic enhancement 3, 4
- Higher flow rates (8 mL/sec) provide superior pancreatic enhancement (129 HU vs 106 HU) and longer tumor-to-pancreas contrast duration (26.4 vs 8.6 seconds) compared to standard 4 mL/sec rates 4
- Total contrast volume typically 150 mL for adults 1, 4
Imaging Phases (Triphasic Protocol)
The NCCN mandates this specific triphasic approach for all patients with suspected pancreatic cancer: 1
Late arterial/pancreatic parenchymal phase: 40-50 seconds post-injection 1, 2, 5
Portal venous phase: 65-70 seconds post-injection 1, 2, 3, 5
- Essential for evaluating venous structures (SMV, splenic vein, portal vein) and detecting metastases 1
Optional non-contrast phase may be included for detecting calcifications and differentiating from chronic pancreatitis 1
Slice Thickness and Reconstruction
- Thin-slice acquisition: ≤3mm axial sections, preferably submillimeter 1, 2
- Allows detection of metastatic deposits as small as 3-5mm 1
- Enables multiplanar reconstruction for assessing tumor-vessel relationships 1
Clinical Rationale
Vascular Assessment
The triphasic protocol enables critical evaluation of: 1, 2
- Arterial structures: celiac axis, superior mesenteric artery, hepatic artery, peripancreatic arteries
- Venous structures: superior mesenteric vein, splenic vein, portal vein
- Vascular invasion assessment for determining resectability (70-85% of CT-determined resectable tumors proceed to successful resection) 1
Tumor Detection and Characterization
- Pancreatic adenocarcinoma demonstrates hypovascular, hypoattenuating appearance with ill-defined margins 3
- Peak pancreatic enhancement occurs at 28.7 seconds with high flow rates, providing optimal tumor conspicuity 4
- Indirect signs include: pancreatic duct dilation, "double duct sign" (biliary and pancreatic duct obstruction), distal parenchymal atrophy 3
Important Caveats and Pitfalls
Isoattenuating Tumors
- 10-15% of pancreatic adenocarcinomas may be isoattenuating and not visible on CT 3
- When CT is non-diagnostic but clinical suspicion remains high, proceed to MRI with diffusion-weighted imaging 1, 3
Contrast Contraindications
- When IV contrast is contraindicated (allergy, renal insufficiency), MRI with gadolinium is the preferred alternative 1, 2
- MRI detects hepatic metastases not visible on CT in 10-23% of cases 3
- Non-contrast MRI with diffusion-weighted imaging is superior to non-contrast CT 2
Limitations
- CT has limited sensitivity for small hepatic and peritoneal metastases 1
- Consider staging laparoscopy in high-risk patients (borderline resectable disease, markedly elevated CA 19-9, large tumors) to detect subradiologic metastases 1
- Concurrent pancreatitis may lead to overestimation of tumor extent 6
Alternative and Complementary Imaging
MRI/MRCP
- MRI is preferred for pancreatic cyst evaluation due to superior soft-tissue contrast and ability to demonstrate ductal communication 1, 2
- For cystic lesions, MRI better identifies mural nodules, septations, and communication with pancreatic duct 1
- Lifelong surveillance of pancreatic cysts should use MRI to avoid cumulative radiation exposure 1
Endoscopic Ultrasound (EUS)
- EUS is complementary to CT for staging, particularly for small tumors and lymph node assessment 1, 6
- EUS-guided FNA is preferable to CT-guided biopsy for resectable disease (better yield, lower peritoneal seeding risk) 1
- However, biopsy is not required before surgical resection when clinical suspicion is high 1