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Palabras claves: páncreas/ neoplasia papilares sólido quísticas/ tumor de Frantz Gruber. This entity is part of the cystic type tumors of the pancreas that affect with higher frequency the tail and body of the organ, prevailing in women and in Histology showed the cell arrangement in a pseudopapillary pattern with few solid areas and extensive cystic changes with presence of hemorrhage and necrosis, suggestive of solid pseudopapillary neoplasm of the pancreas, namely, a Gruber Frantz tumor (Figures F,G). This is the rarest cystic neoplasm of the pancreas, with an incidence of 0.17%–2.5%. The Gruber-Frantz tumor or solid pseudopapillary tumor of the pancreas accounts for 1% to 2% of pancreatic tumors. It occurs more frequently among wom… The Frantz tumor (solid pseudopapillary neoplasm – SPN) is a rare, usually benign tumor of unclear etiology having a predilection for young women.

solid papillary epithelial neoplasm. solid-pseudopapillary tumour of the pancreas. 2020-10-26 DISCUSSION: Frantz-Gruber tumor is a rare pancreatic tumor suspected during the evaluation of a young female with abdominal pain and confirmed during surgery. It is important to consider the existence of this tumor in the evaluation of patients with these characteristics; even if the tumor's biological behavior is benign Frantz-Gruber tumor is considered a low-grade malignant tumor The Frantz tumor (synonyms: solid pseudopapillary neoplasm, SPN, solid pseudopapillary tumor) is an uncommon pancreatic neoplasm with low-metastatic potential, which occurs mainly in young women.

It comprises 1-2% of non-endocrine Deze tumor wordt ook wel Hamoudi tumor of Gruber-Frantz tumor genoemd.

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It is considered to be a low-grade malignancy of pancreas and mostly occurs in middle-aged women. The topic Gruber-Frantz Tumor you are seeking is a synonym, or alternative name, or is closely related to the medical condition Pseudopapillary Tumor of Pancreas.

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In 1996, the World Health Organization (WHO) has renamed it as "solid pseudopapillary tumor" for the international It is considered to be a low-grade malignancy of pancreas and mostly occurs in middle-aged women. The topic Gruber-Frantz Tumor you are seeking is a synonym, or alternative name, or is closely related to the medical condition Pseudopapillary Tumor of Pancreas. Quick Summary: The result of treatment of a young female patient with solid pseudopapillary tumor of the pancreas is reported. This tumor is extremely rare and is revealed, as a rule, accidentally during periodic screening or when the tumor achieves the large size. The presence of a cyst on the pancreas should be considered, in particular, from the position of possible detection of a solid pseudopapillary tumor. Rare case of solid pseudopapillary pancreatic tumour (Gruber-Frantz tumour) Request PDF | Gruber-Frantz tumor: A very rare pathological condition in children | Solid pseudopapillary tumor of the pancreas or Gruber-Frantz tumor is a rare pathological entity. Its incidence Solid pseudopapillary tumor (SPT) or neoplasm (SPN), also named papillary epithelial neoplasm or Frantz tumor (also Gruber-Frantz or rarely Hamoudi tumor) is a low-grade or borderline epithelial pancreatic malignancy and has been reported in 0.9-2.7% of all neoplasms of the pancreas often characterized as a rather large one, presenting mixed morphology (1).

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Rare case of solid pseudopapillary pancreatic tumour (Gruber-Frantz tumour) Request PDF | Gruber-Frantz tumor: A very rare pathological condition in children | Solid pseudopapillary tumor of the pancreas or Gruber-Frantz tumor is a rare pathological entity. Its incidence Solid pseudopapillary tumor (SPT) or neoplasm (SPN), also named papillary epithelial neoplasm or Frantz tumor (also Gruber-Frantz or rarely Hamoudi tumor) is a low-grade or borderline epithelial pancreatic malignancy and has been reported in 0.9-2.7% of all neoplasms of the pancreas often characterized as a rather large one, presenting mixed morphology (1). 2019-01-03 Frantz-Gruber tumor: a case report. Rev Gastroenterol Mex 2004; 69(4): 235-238.

They are rare and thought to account for 1-2% of exocrine pancreatic tumours. They tend to present in young non-Caucasian females around the 2 nd and 3 rd decades of life (the 'daughter' tumour) 10.
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Originally described by Franz in 1959, its origin name was a Franz-Gruber tumor. It has a number of imaging characteristics, as well as demographic aspects common to this rare pancreatic tumor.

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Facebook gives people the power to The Frantz-Gruber tumor is a rare solid pseudopapilar mass of the pancreas characterized for its low malignant potential, first described by Franz in 1959.1 It occurs mainly in women between the third and fourth decades of life. Symptoms are determined by a mass effect, commonly non-specific abdominal pain and fullness sensation. Tumor de Frantz é definido como um tumor sólido pseudopapilar do pâncreas descrito pela primeira vez em 1959.

Freda F, Procaccini E, Ruggiero R, Antropoli M, Manganiello A, Nunziata L, Petronella P, Lo Schiavo F. Solid-cystic pseudopapillary tumor of pancreas: description of two cases and literature review. The preoperative diagnosis of a solid pseudo-papillary tumor (Gruber-Frantz tumor) was made, based on ultrasonography and computed tomography. Laparoscopic resection was decided upon based on the fact that there were clearly defined surgical planes despite of the size of the mass. Gruber-Frantz tumour is a rare cystic neoplasm of the pancreas that is most frequently seen in young females. Cystic pancreatic neoplasms are commonly misdiagnosed as pancreatic pseudocysts that are, by far, the most common cystic lesions of the pancreas.