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Papillary cystic and solid tumour of the pancreas: Report of a case and literature review

BACKGROUND: The papillary cystic and solid tumour of the pancreas (PCSTP) is a rare primary neoplasm of unknown pathogenesis typically found in young women. PCSTP is a low-grade malignant tumour, which is often asymptomatic but it may present with abdominal pain. CASE PRESENTATION: A 38 year old fem...

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Detalles Bibliográficos
Autores principales: Kasem, Abdul, Ali, Zainab, Ellul, Joseph
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1261538/
https://www.ncbi.nlm.nih.gov/pubmed/16188022
http://dx.doi.org/10.1186/1477-7819-3-62
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author Kasem, Abdul
Ali, Zainab
Ellul, Joseph
author_facet Kasem, Abdul
Ali, Zainab
Ellul, Joseph
author_sort Kasem, Abdul
collection PubMed
description BACKGROUND: The papillary cystic and solid tumour of the pancreas (PCSTP) is a rare primary neoplasm of unknown pathogenesis typically found in young women. PCSTP is a low-grade malignant tumour, which is often asymptomatic but it may present with abdominal pain. CASE PRESENTATION: A 38 year old female patient who presented with one day history of epigastric pain was diagnosed as PCSTP. The patient was successfully treated with distal pancreatectomy. CONCLUSION: It is important to differentiate this tumour from other pancreatic tumours because, unlike malignant pancreatic tumours, this neoplasm does not usually metastasise and is amenable to cure after complete surgical resection. However, the cell origin and the aetiology of this tumour are not clear and further studies are warranted in its pathogenesis.
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spelling pubmed-12615382005-10-22 Papillary cystic and solid tumour of the pancreas: Report of a case and literature review Kasem, Abdul Ali, Zainab Ellul, Joseph World J Surg Oncol Case Report BACKGROUND: The papillary cystic and solid tumour of the pancreas (PCSTP) is a rare primary neoplasm of unknown pathogenesis typically found in young women. PCSTP is a low-grade malignant tumour, which is often asymptomatic but it may present with abdominal pain. CASE PRESENTATION: A 38 year old female patient who presented with one day history of epigastric pain was diagnosed as PCSTP. The patient was successfully treated with distal pancreatectomy. CONCLUSION: It is important to differentiate this tumour from other pancreatic tumours because, unlike malignant pancreatic tumours, this neoplasm does not usually metastasise and is amenable to cure after complete surgical resection. However, the cell origin and the aetiology of this tumour are not clear and further studies are warranted in its pathogenesis. BioMed Central 2005-09-27 /pmc/articles/PMC1261538/ /pubmed/16188022 http://dx.doi.org/10.1186/1477-7819-3-62 Text en Copyright © 2005 Kasem et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kasem, Abdul
Ali, Zainab
Ellul, Joseph
Papillary cystic and solid tumour of the pancreas: Report of a case and literature review
title Papillary cystic and solid tumour of the pancreas: Report of a case and literature review
title_full Papillary cystic and solid tumour of the pancreas: Report of a case and literature review
title_fullStr Papillary cystic and solid tumour of the pancreas: Report of a case and literature review
title_full_unstemmed Papillary cystic and solid tumour of the pancreas: Report of a case and literature review
title_short Papillary cystic and solid tumour of the pancreas: Report of a case and literature review
title_sort papillary cystic and solid tumour of the pancreas: report of a case and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1261538/
https://www.ncbi.nlm.nih.gov/pubmed/16188022
http://dx.doi.org/10.1186/1477-7819-3-62
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