Dramatic 5 x 7 cm mixed hypoechoic region of the right pancreatic limb is noted with hyperechoic ill-defined surrounding tissue consistent with saponification of fat (Image 1). A trace of free fluid is noted in the 11 O’clock position. Video of the same right pancreatic limb demonstrating the extension of the mixed hypoechoic pathology in a tubular shape that would help lead to suspect pancreatic origin (Video 1). Some small focal echogenic pinpoint changes are present at 3 O’clock that may represent early mineralization or fibrosis. Linear high resolution image of the same right pancreatic limb utilizing harmonics in order to filter interfering echoes and provide better detail to the image (Video 2). Power Doppler assessment of the right pancreatic pathology demonstrating strong central signals indicating primary blood flow to the region combined with areas devoid of Doppler signals leading to suspect regional necrosis or sequestrum (Video 3). Video demonstrating a 22-gauge US-guided fine needle aspirate (FNA) of the hypoechoic region of the pathology (Video 4). In this case the sonographer draws back on the syringe attempting to aspirate fluid in case of abscessation. Given that no coalesced fluid was present, the jab technique was then used without drawing back on the syringe in Video 5. The jab technique of the solid tissue is used to gently push the pathological cells into the needle hub; which is gently sprayed onto a slide. No aspiration actually occurs during sampling. Three days later after the cytology had been assessed, US-guided biopsy was performed to confirm the cytological interpretation and ensure no neoplasia was present (Video 6). The core biopsy needle is first seated into the pathology at the 2 O’clock position (hyperechoic focus just beneath the pancreatic capsule on the screen.) A 14-gauge 2.2 cm spring loaded core biopsy is taken of variable echogenicities within the pathology (Video 7). Note that the needle passes through both dramatically hypoechoic, mildly hypoechoic, and hyperechoic changes within the pancreatic limb in order to provide the pathologist with a variety of information (matched with the variety of sampled echogenicities) for the sample interpretation. The needle extends to a point 1cm proximal to the hyperechoic granulation bed in the far field at the 6 O’clock position to ensure that passage beyond the pancreatic capsule (buried under the hyperechoic bordering changes) does not occur. The pathology is unchanged post biopsy other than a slight interruption of the hyperechoic capsule in the near field where the biopsy needle entered the pancreas at the 12 O’clock position (Video 8). No free fluid is noted that would indicate post sampling hemorrhage immediately post biopsy nor after 5 minutes shown in Video 9. The sonographer applies direct pressure to any tissue that he samples by biopsy for approximately 3 minutes as a security measure to avoid excessive bleeding.