Solid pseudopapillary neoplasm of the pancreas. (Frantz´s tumor) Anatomo-clinical aspects.

Authors

DOI:

https://doi.org/10.31837/cir.urug/7.1.3

Keywords:

Frantz tumor, neuroendocrine tumors, pancreas, pancreatectomy

Abstract

Pseudo papillary tumor of the pancreas, also called Frantz´s tumor, is a very rare disease; between 0.2 and 2.7% of pancreatic carcinomas. Ethiology is unknown; is observed in young women. It´s a tumors with low malignant potential, usually of asymptomatic evolution by long time and the symptoms are due to regional compression: pain or abdominal mass. The possibility of a malignant form is around 15%.

Anatomically, they are most frequently located in the tail of the pancreas, followed by the head and body. The treatment is the surgical resection; with an excellent prognosis and a 5-year survival almost 100%.

The diagnosis is with pathological study, considering the microscopic appearance and the immunohistochemical profile. Its perform an analysis of the literature and once case of a 21 years old, woman is reported. A complete resection surgery of the tumor was performed and remains asymptomatic at 24 months of follow-up.

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Published

2023-04-26

How to Cite

1.
Marrero G, Campos M, Laca E, González D, Ruso Martínez L. Solid pseudopapillary neoplasm of the pancreas. (Frantz´s tumor) Anatomo-clinical aspects. Cir. Urug. [Internet]. 2023 Apr. 26 [cited 2024 May 16];7(1):ecir.urug.7.1.3. Available from: https://revista.scu.org.uy/index.php/cir_urug/article/view/5730

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