𝔖 Bobbio Scriptorium
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Papillary-cystic neoplasm of the pancreas

✍ Scribed by Christopher M. Pezzi; Conrad Schuerch; Robert A. Erlandson; John Deitrick


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
557 KB
Volume
37
Category
Article
ISSN
0022-4790

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✦ Synopsis


Papillary-cystic neoplasm of the pancreas is a rare tumor which has recently been described as a distinct, clinicopathological entity. Forty-four previously described cases from the literature and an additional 52 cases referred to in a brief abstract are reviewed. An additional case occurring in a 25-year-old woman is reported. This tumor occurs primarily in young women (mean age 23.3 years) and presents as a large abdominal mass (mean size 10.3 cm) in 63% of patients. Treatment is surgical resection of the involved portions of the pancreas and results of treatment are excellent following this form of therapy alone. The tumor appears to represent a low-grade malignancy, possibly of ductal cell origin. Only two patients with recurrences and two patients with metastatic disease have been reported. Surgeons should be aware of this curable pancreatic malignancy as they are most often responsible for the evaluation and treatment of the patient presenting with a large abdominal mass.


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## Abstract Papillary‐cystic carcinoma of the pancreas is an extremely rare tumor which occurs in young adults, may invade locally, but is late to metasta‐size. As opposed to adenocarcinoma of the pancreas, portal vein invasion should not be included as a criteria for nonresectability. In the absen