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. The disease prognosis is favorable, recurrence is rare.

Solid pseudopapillary tumor of the pancreas or Gruber-Frantz tumor is a rare pathological entity. Its incidence is even lower in children. This neoplasm has low malignant potential and with adequate surgical treatment has a very good prognosis. We present the case of a 15-year-old girl admitted in our department for an intra-abdominal tumor, diagnosed incidentally on ultrasonography after a

This neoplasm has low malignant potential and with adequate surgical treatment has a very good prognosis. We present the case of a 15-year-old girl admitted in our department for an intra-abdominal tumor, diagnosed incidentally on ultrasonography after a minor trauma. 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 neoplasm, solid and cystic tumor of acinar cells and finally the Gruber-Frantz tumor (Frantz-Gruber), make it difficult to estimate the frequency of the occurrence of tumors, so the real level data SPPT is difficult to assess. In 1996, the World Health Organization (WHO) has renamed it as "solid pseudopapillary tumor" for the international Background: Solid cystic pseudopapillary tumor of the pancreas (SCPTP), commonly known as Gruber-Frantz’s tumor is a rare form of pancreatic tumors commonly misdiagnosed as pancreatic pseudocysts. It mainly affects middle-aged women, with an excellent prognosis. Pseudopapillary Tumor of Pancreas is a rare, malignant cancer that forms in the exocrine pancreas.

4. 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.

15 Jul 2019 Tumor de Frantz: Neoplasia Sólida Pseudopapilar de Páncreas, Juan Frantz- Gruber Tumor: revisión en relación a un caso, Autores: Dr

BM R Madzhov, R Gaidarski, P Arnaudov, P Chernopolski, T Ivanov, M Tsaneva. Khirurgiia solid and papillary neoplasm of the pancreas , papillary cystic tumor [1-4].

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. The disease prognosis is favorable, recurrence is rare.

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. This usually asymptomatic tumor may, however, be a cause of abdominal pain or discomfort.

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 neoplasm, solid and cystic tumor of acinar cells and finally the Gruber-Frantz tumor (Frantz-Gruber), make it difficult to estimate the frequency of the occurrence of tumors, so the real level data SPPT is difficult to assess. In 1996, the World Health Organization (WHO) has renamed it as "solid pseudopapillary tumor" for the international Background: Solid cystic pseudopapillary tumor of the pancreas (SCPTP), commonly known as Gruber-Frantz’s tumor is a rare form of pancreatic tumors commonly misdiagnosed as pancreatic pseudocysts.
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solid and pseudopapillary epithelial neoplasm. Frantz’s tumor. 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.

25 Oct 2012 Keywords: Frantz′s tumor, pancreatic tumors, solid cystic papillary neoplasms solid and cystic acinar cell tumor and Gruber-Frantz's tumor. Anatomic Pathology / p120 in Solid pSeudopapillary TumorS of pancreaS p120 Catenin known as the Gruber-Frantz tumor.11 It is an uncommon, low-grade This tumor was known by various names like Gruber-Frantz tumor, solid and cystic tumor, solid and papillary epithelial neoplasm, papillary cystic tumor and solid- 21 Jul 2011 Gruber-Frantz tumour is a rare cystic neoplasm of the pancreas that is most frequently seen in young females.
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Background: Solid cystic pseudopapillary tumor of the pancreas (SCPTP), commonly known as Gruber-Frantz’s tumor is a rare form of pancreatic tumors commonly misdiagnosed as pancreatic pseudocysts. It mainly affects middle-aged women, with an excellent prognosis.

Its incidence exploratoria para excéresis del tumor mediante pancreatectomia . 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%.

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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).

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. This usually asymptomatic tumor may, however, be a cause of abdominal pain or discomfort. Other names include solid pseudopapillary tumor (SPT) of the pancreas, solid pseudopapillary neoplasm (SPN), papillary cystic neoplasm of the pancreas, Hamoudi tumor, or Gruber-Frantz tumor.