Cystic Pancreatic Lesions

Serous Cystic Neoplasm


          Serous cystic adenomas contain multiple small cysts resulting in a lobulated contour. Some have a central scar with calcifications.

          Benign tumor, but large tumors have a tendency to increase in size and cause symptoms

          Typically seen after 60 years of age

          Microcystic or honey-combed cyst with central scar (30%) and calcifications (18%)

          Macrocystic in 10% and difficult to differentiate from pseudocyst and mucinous cystic neoplasm

          Lobulated surface

          No communication between cysts and pancreatic duct.

          Hypervascular enhancement is sometimes seen and can look like cystic neuroendocrine tumor

          Growth rate of tumors Growth rate of tumors > 4 cm: up to 20 mm/y


Mucinous Cystic Neoplasm


          Premalignant tumor - may transform into a Mucinous Cystadenocarcinoma

          Exclusively seen in women - Median age: 40-50 years

          Macrocystic with thick wall septations and peripheral calcifications

          Peripheral calcifications seen in 25%. This finding allows you to make a specific diagnosis

          Location in the tail and body of the pancreas (95%).

          Most are symptomatic, presenting with nondescript abdominal pain



Intraductal Papillary Mucinous Neoplasm


          Mucin producing tumor in main pancreatic duct or branch-duct.

          Location: pancreatic head >> tail and body.

          Must have communication with pancreatic duct. Best seen with MRCP.

          Can be multifocal.

          Main-duct IPMN has imaging features distinct from branch-type.

          Branch-duct type can look like other cystic neoplasms


Signs of malignancy are:

          Pancreatic duct > 8 mm - as in this case.

          Solid node in duct.

          Mass around the pancreatic duct.

          Enlarged choledochal duct.


Solid Pseudopapillary Neoplasm


          Very uncommon neoplasm seen in women 20-30 years.

          Solid and cystic neoplasm with capsule and with early 'hemangioma-like' enhancement. Sometimes intratumoral hemorrhage


Neuroendocrine tumor with cystic degeneration


          Non-functioning endocrine neoplasm

          Islet cell tumor

          Hypervascular with ring-enhancement. This is unlike serous cystic neoplasms that enhance from the center and more solid)