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Pancreatic pseudopapillary tumour: A rare misdiagnosed entity

INTRODUCTION: Solid pseudo papillary pancreatic tumour is a rare entity. The atypical presentation causes a delayed or misdiagnosis of these pathology. It commonly affects the female population in the 2nd and 3rd decade of life. The presentation varies from non-specific abdominal pain to incidental...

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Detalles Bibliográficos
Autores principales: Affirul, C.A., Qisti, F.N., Zamri, Z., Azlanuddin, A., Hairol, A.O., Razman, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245679/
https://www.ncbi.nlm.nih.gov/pubmed/25462046
http://dx.doi.org/10.1016/j.ijscr.2014.09.021
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author Affirul, C.A.
Qisti, F.N.
Zamri, Z.
Azlanuddin, A.
Hairol, A.O.
Razman, J.
author_facet Affirul, C.A.
Qisti, F.N.
Zamri, Z.
Azlanuddin, A.
Hairol, A.O.
Razman, J.
author_sort Affirul, C.A.
collection PubMed
description INTRODUCTION: Solid pseudo papillary pancreatic tumour is a rare entity. The atypical presentation causes a delayed or misdiagnosis of these pathology. It commonly affects the female population in the 2nd and 3rd decade of life. The presentation varies from non-specific abdominal pain to incidental findings in asymptomatic patients. It is a low-grade premalignant condition that is curable by excision of the tumour. PRESENTATION OF CASE: This paper presents a 17-year-old girl with intra-abdominal mass diagnosed with solid pseudo papillary tumour that underwent Whipple's procedure. DISCUSSION: We discuss the presentations, diagnosis and pathology findings of this rare pathology. CONCLUSION: The diagnosis remains an enigma in view of the nature and location of the tumour. Resection is still the best choice remains for this condition.
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spelling pubmed-42456792014-12-03 Pancreatic pseudopapillary tumour: A rare misdiagnosed entity Affirul, C.A. Qisti, F.N. Zamri, Z. Azlanuddin, A. Hairol, A.O. Razman, J. Int J Surg Case Rep Article INTRODUCTION: Solid pseudo papillary pancreatic tumour is a rare entity. The atypical presentation causes a delayed or misdiagnosis of these pathology. It commonly affects the female population in the 2nd and 3rd decade of life. The presentation varies from non-specific abdominal pain to incidental findings in asymptomatic patients. It is a low-grade premalignant condition that is curable by excision of the tumour. PRESENTATION OF CASE: This paper presents a 17-year-old girl with intra-abdominal mass diagnosed with solid pseudo papillary tumour that underwent Whipple's procedure. DISCUSSION: We discuss the presentations, diagnosis and pathology findings of this rare pathology. CONCLUSION: The diagnosis remains an enigma in view of the nature and location of the tumour. Resection is still the best choice remains for this condition. Elsevier 2014-10-07 /pmc/articles/PMC4245679/ /pubmed/25462046 http://dx.doi.org/10.1016/j.ijscr.2014.09.021 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Affirul, C.A.
Qisti, F.N.
Zamri, Z.
Azlanuddin, A.
Hairol, A.O.
Razman, J.
Pancreatic pseudopapillary tumour: A rare misdiagnosed entity
title Pancreatic pseudopapillary tumour: A rare misdiagnosed entity
title_full Pancreatic pseudopapillary tumour: A rare misdiagnosed entity
title_fullStr Pancreatic pseudopapillary tumour: A rare misdiagnosed entity
title_full_unstemmed Pancreatic pseudopapillary tumour: A rare misdiagnosed entity
title_short Pancreatic pseudopapillary tumour: A rare misdiagnosed entity
title_sort pancreatic pseudopapillary tumour: a rare misdiagnosed entity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245679/
https://www.ncbi.nlm.nih.gov/pubmed/25462046
http://dx.doi.org/10.1016/j.ijscr.2014.09.021
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