Zobrazeno 1 - 10
of 187
pro vyhledávání: '"Solid pseudopapillary tumour"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 22, Iss C, Pp 5-8 (2017)
A solid pseudopapillary tumour (SPT) of the pancreas is very rare in children. Despite its malignancy potential, SPT is known to have a good prognosis. No prior report has described the use of neoadjuvant chemoradiation with retinoid therapy for size
Externí odkaz:
https://doaj.org/article/e5101b8f1f6740d2a049f08265018cab
Akademický článek
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Akademický článek
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Autor:
Nihed Abdessaied, Ali Ben Ali, Waad Farhat, Houssem Ammar, Amal Bouazzi, Mohamed Ben Mabrouk, Abdelkader Mizouni, Mohamed Amine Said
Publikováno v:
ANZ Journal of Surgery. 90:1683-1688
Background Solid pseudopapillary tumour of the pancreas (SPTP) is a rare pancreatic tumour characterized by a non-specific clinical presentations and vague radiologic features. The aim of this study is to identify these tumours from other pancreatic
Publikováno v:
Current Medicine Research and Practice, Vol 2, Iss 4, Pp 227-231 (2012)
Frantz tumour or solid pseudopapillary tumour (SPT) of the pancreas is a rare clinical entity which predominantly affects young women in their second and third decades of life. Due to paucity of number of cases, the natural history of the disease is
Externí odkaz:
https://doaj.org/article/9b0acb16c330409f9b1a0e90d7b97634
Publikováno v:
Videosurgery and Other Miniinvasive Techniques, Vol 5, Iss 2, Pp 65-69 (2010)
Solid pseudopapillary tumour (Frantz tumour) is a rare primary neoplasm of the pancreas. We report our experiencewith LDP in two cases of children with Frantz tumour. Two patient cases were reviewed. In both laparoscopy was carriedout. There were no
Externí odkaz:
https://doaj.org/article/da1397baf5084f7796514bc7698c395e
Publikováno v:
Indian Journal of Pathology and Oncology. 7:477-479
Introduction: Solid Pseudopapillary tumor (SPT) is a tumor with low malignant potential and comprises around 1-2% of all tumors occurring in Pancreas. Pseudocyst of Pancreas, Microcystic adenoma, neuroendocrine tumor and mucinous cystic neoplasm are
Publikováno v:
Ann R Coll Surg Engl
Solid pseudopapillary tumours of the pancreas and giant splenic cysts are very rare entities, and their coexistence in a young female patient has not been previously reported in the literature. We present the case of a 27-year-old woman who presented
Autor:
Carmela Brillantino, Massimo Zeccolini, Pietro Pirisi, Eugenio Rossi, Maria Elena Errico, Rocco Minelli, Raffaele Zeccolini, Giovanni Gaglione, Biagio F Menna
Publikováno v:
J Ultrasound
Pseudopapillary solid tumour of the pancreas is a rare neoplasm that mainly affects young women in the second and third decade of life and less frequently children; originates from the exocrine component of the pancreas; and is characterized by slow
Publikováno v:
African Journal of Paediatric Surgery, Vol 5, Iss 2, Pp 87-89 (2008)
The solid pseudopapillary tumour (SPT) of the pancreas is an uncommon cystic pancreatic neoplasm mostly seen in young females. We present a large SPT in a 16-year-old female who presented with acute onset upper- and mid-quadrant abdominal pain associ
Externí odkaz:
https://doaj.org/article/afafe87d37a14a02bb1fb3c3a70e975d