TY - JOUR
T1 - Primary pancreatic cystic neoplasms of the pancreas revisited. Part IV
T2 - Rare cystic neoplasms
AU - Sakorafas, George H.
AU - Smyrniotis, Vasileios
AU - Reid-Lombardo, Kaye M.
AU - Sarr, Michael G.
PY - 2012/9/1
Y1 - 2012/9/1
N2 - Primary pancreatic cystic neoplasms are being recognized with increasing frequency due to modern imaging techniques. In addition to the more common cystic neoplasms - serous cystadenoma, primary mucinous cystic neoplasm, and intraductal papillary mucinous neoplasm - there are many other less common neoplasms that appear as cystic lesions. These cystic neoplasms include solid pseudopapillary neoplasm of the pancreas (the most common rare cystic neoplasm), cystic neuroendocrine neoplasm, cystic degeneration of otherwise solid neoplasms, and then the exceedingly rare cystic acinar cell neoplasm, intraductal tubular neoplasm, angiomatous neoplasm, lymphoepithelial cysts (not true neoplasms), and few others of mesenchymal origin. While quite rare, the pancreatic surgeon should at the least consider these unusual neoplasms in the differential diagnosis of potentially benign or malignant cystic lesions of the pancreas. Moreover, each of these unusual neoplasms has their own natural history/tumor biology and may require a different level of operative aggressiveness to obtain the optimal outcome.
AB - Primary pancreatic cystic neoplasms are being recognized with increasing frequency due to modern imaging techniques. In addition to the more common cystic neoplasms - serous cystadenoma, primary mucinous cystic neoplasm, and intraductal papillary mucinous neoplasm - there are many other less common neoplasms that appear as cystic lesions. These cystic neoplasms include solid pseudopapillary neoplasm of the pancreas (the most common rare cystic neoplasm), cystic neuroendocrine neoplasm, cystic degeneration of otherwise solid neoplasms, and then the exceedingly rare cystic acinar cell neoplasm, intraductal tubular neoplasm, angiomatous neoplasm, lymphoepithelial cysts (not true neoplasms), and few others of mesenchymal origin. While quite rare, the pancreatic surgeon should at the least consider these unusual neoplasms in the differential diagnosis of potentially benign or malignant cystic lesions of the pancreas. Moreover, each of these unusual neoplasms has their own natural history/tumor biology and may require a different level of operative aggressiveness to obtain the optimal outcome.
KW - Acinar cell neoplasm
KW - Choriocarcinoma
KW - Cystic lymphangioma
KW - Cystic neoplasms of pancreas
KW - Hemangioma
KW - Intraductal tubular neoplasm
KW - Neuroendocrine neoplasm
KW - Pseudopapillary neoplasm of the pancreas
KW - Teratoma
UR - http://www.scopus.com/inward/record.url?scp=84864707450&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864707450&partnerID=8YFLogxK
U2 - 10.1016/j.suronc.2011.06.007
DO - 10.1016/j.suronc.2011.06.007
M3 - Review article
C2 - 21816607
AN - SCOPUS:84864707450
SN - 0960-7404
VL - 21
SP - 153
EP - 163
JO - Surgical Oncology
JF - Surgical Oncology
IS - 3
ER -