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Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy
BACKGROUND: Acinar cell carcinoma (ACC) represents only 1–2% of pancreatic cancers and is a very rare malignancy. At the time of diagnosis only 50% of the tumors appear to be resectable. Reliable data for an effective adjuvant or neoadjuvant treatment are not available. CASE PRESENTATION: A 65-year...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657786/ https://www.ncbi.nlm.nih.gov/pubmed/19239719 http://dx.doi.org/10.1186/1477-7819-7-22 |
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author | Distler, Marius Rückert, Felix Dittert, Dag D Stroszczynski, Christian Dobrowolski, Frank Kersting, Stephan Grützmann, Robert |
author_facet | Distler, Marius Rückert, Felix Dittert, Dag D Stroszczynski, Christian Dobrowolski, Frank Kersting, Stephan Grützmann, Robert |
author_sort | Distler, Marius |
collection | PubMed |
description | BACKGROUND: Acinar cell carcinoma (ACC) represents only 1–2% of pancreatic cancers and is a very rare malignancy. At the time of diagnosis only 50% of the tumors appear to be resectable. Reliable data for an effective adjuvant or neoadjuvant treatment are not available. CASE PRESENTATION: A 65-year old male presented with obstructive jaundice and non-specific upper abdominal pain. MRI-imaging showed a tumor within the head of the pancreas concomitant with Serum-Lipase and CA19-9. During ERCP, a stent was placed. Endosonographic fine needle biopsy confirmed an acinar cell carcinoma. Laparotomy presented an locally advanced tumor with venous infiltration that was consequently deemed unresectable. The patient was treated with five cycles of 5-FU monotherapy with palliative intention. Chemotherapy was well tolerated, and no severe complications were observed. Twelve months later, the patient was in stable condition, and CT-scanning showed an obvious reduction in the size of the tumor. During further operative exploration, a PPPD with resection of the portal vein was performed. Histopathological examination gave evidence of a diffuse necrotic ACC-tumor, all resection margins were found to be negative. Eighteen months later, the patient showed no signs of recurrent disease. CONCLUSION: ACC responded well to 5-FU monochemotherapy. Therefore, neoadjuvant chemotherapy could be an option to reduce a primarily unresectable ACC to a point where curative resection can be achieved. |
format | Text |
id | pubmed-2657786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26577862009-03-19 Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy Distler, Marius Rückert, Felix Dittert, Dag D Stroszczynski, Christian Dobrowolski, Frank Kersting, Stephan Grützmann, Robert World J Surg Oncol Case Report BACKGROUND: Acinar cell carcinoma (ACC) represents only 1–2% of pancreatic cancers and is a very rare malignancy. At the time of diagnosis only 50% of the tumors appear to be resectable. Reliable data for an effective adjuvant or neoadjuvant treatment are not available. CASE PRESENTATION: A 65-year old male presented with obstructive jaundice and non-specific upper abdominal pain. MRI-imaging showed a tumor within the head of the pancreas concomitant with Serum-Lipase and CA19-9. During ERCP, a stent was placed. Endosonographic fine needle biopsy confirmed an acinar cell carcinoma. Laparotomy presented an locally advanced tumor with venous infiltration that was consequently deemed unresectable. The patient was treated with five cycles of 5-FU monotherapy with palliative intention. Chemotherapy was well tolerated, and no severe complications were observed. Twelve months later, the patient was in stable condition, and CT-scanning showed an obvious reduction in the size of the tumor. During further operative exploration, a PPPD with resection of the portal vein was performed. Histopathological examination gave evidence of a diffuse necrotic ACC-tumor, all resection margins were found to be negative. Eighteen months later, the patient showed no signs of recurrent disease. CONCLUSION: ACC responded well to 5-FU monochemotherapy. Therefore, neoadjuvant chemotherapy could be an option to reduce a primarily unresectable ACC to a point where curative resection can be achieved. BioMed Central 2009-02-25 /pmc/articles/PMC2657786/ /pubmed/19239719 http://dx.doi.org/10.1186/1477-7819-7-22 Text en Copyright © 2009 Distler 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 Distler, Marius Rückert, Felix Dittert, Dag D Stroszczynski, Christian Dobrowolski, Frank Kersting, Stephan Grützmann, Robert Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
title | Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
title_full | Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
title_fullStr | Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
title_full_unstemmed | Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
title_short | Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
title_sort | curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657786/ https://www.ncbi.nlm.nih.gov/pubmed/19239719 http://dx.doi.org/10.1186/1477-7819-7-22 |
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