Whereas pancreatic duct adenocarcinoma (PDA) is a well-studied (but still poorly understood) disease with a dismal prognosis, cystic neoplasms of the pancreas form a more recently recognized group of pancreatic tumors. They are diverse and variable in their pathologic characteristics, clinical course, and outcomes, 1-3 although all portend a better overall prognosis than PDA. In recent years, with the improved sensitivity and increasing use of cross-sectional imaging in clinical practice, these lesions are more commonly identified, 4 with many being discovered incidentally. Indeed, large radiological series using computed tomography (CT) or magnetic resonance imaging (MRI) have reported detection rates of pancreatic cystic lesions between 1.2% and almost 20%, 5,6 approaching the 24.3% prevalence rate in an autopsy series by Kimura and colleagues. 7 Although most of these lesions are pseudocysts, a significant portion consist of cystic neoplasms, which are estimated to represent 10% to 15% of all primary pancreatic cystic lesions. 8 Given the growing clinical relevance of these tumors, a keen understanding of their natural history and pathophysiology is needed. This article reviews pancreatic cystic neoplasms, with a focus on the challenges encountered in their diagnosis and treatment.
KeywordsPancreatic cystic neoplasm; Serous cystic neoplasm; Mucinous cystic neoplasm; Intraductal Papillary mucinous neoplasm
Pancreatic Cystic NeoplasmsAlthough pancreatic cystic neoplasms (PCNs) are often discussed together, it is important to realize that they are a heterogeneous group of tumors with wide-ranging malignant potential,