A case of gangliocytic paraganglioma in the ampulla of Vater
<p>Abstract</p> <p>Background</p> <p>Duodenal gangliocytic paraganglioma is an extremely rare tumor and few cases have been reported to date.</p> <p>Case presentation</p> <p>The authors report a case of gangliocytic paraganglioma verified by post...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
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BMC
2010-05-01
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Series: | World Journal of Surgical Oncology |
Online Access: | http://www.wjso.com/content/8/1/42 |
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author | Jang Jin-Young Kang Mee Lee Seung Kwon Junsik Kim Sun-Whe |
author_facet | Jang Jin-Young Kang Mee Lee Seung Kwon Junsik Kim Sun-Whe |
author_sort | Jang Jin-Young |
collection | DOAJ |
description | <p>Abstract</p> <p>Background</p> <p>Duodenal gangliocytic paraganglioma is an extremely rare tumor and few cases have been reported to date.</p> <p>Case presentation</p> <p>The authors report a case of gangliocytic paraganglioma verified by post-op pathology after pancreaticoduodenectomy for a tumor in the ampulla of Vater. The 56-year-old male patient concerned visited our emergency room with melena that started one week prior to hospitalization. The patient was diagnosed to have a tumor in the ampulla of Vater with bleeding on its surface. However post-op, he was diagnosed as having gangliocytic paraganglioma by immunohistochemistry.</p> <p>Conclusion</p> <p>This tumor has precise clinical implications, and if continuous follow up is conducted after careful diagnosis and surgical treatment, invasive major operations, such as, radical pancreaticoduodenectomy can be avoided.</p> |
first_indexed | 2024-12-14T01:30:44Z |
format | Article |
id | doaj.art-e8a443fedfd6466e8d8e491ff5ff0668 |
institution | Directory Open Access Journal |
issn | 1477-7819 |
language | English |
last_indexed | 2024-12-14T01:30:44Z |
publishDate | 2010-05-01 |
publisher | BMC |
record_format | Article |
series | World Journal of Surgical Oncology |
spelling | doaj.art-e8a443fedfd6466e8d8e491ff5ff06682022-12-21T23:22:03ZengBMCWorld Journal of Surgical Oncology1477-78192010-05-01814210.1186/1477-7819-8-42A case of gangliocytic paraganglioma in the ampulla of VaterJang Jin-YoungKang MeeLee SeungKwon JunsikKim Sun-Whe<p>Abstract</p> <p>Background</p> <p>Duodenal gangliocytic paraganglioma is an extremely rare tumor and few cases have been reported to date.</p> <p>Case presentation</p> <p>The authors report a case of gangliocytic paraganglioma verified by post-op pathology after pancreaticoduodenectomy for a tumor in the ampulla of Vater. The 56-year-old male patient concerned visited our emergency room with melena that started one week prior to hospitalization. The patient was diagnosed to have a tumor in the ampulla of Vater with bleeding on its surface. However post-op, he was diagnosed as having gangliocytic paraganglioma by immunohistochemistry.</p> <p>Conclusion</p> <p>This tumor has precise clinical implications, and if continuous follow up is conducted after careful diagnosis and surgical treatment, invasive major operations, such as, radical pancreaticoduodenectomy can be avoided.</p>http://www.wjso.com/content/8/1/42 |
spellingShingle | Jang Jin-Young Kang Mee Lee Seung Kwon Junsik Kim Sun-Whe A case of gangliocytic paraganglioma in the ampulla of Vater World Journal of Surgical Oncology |
title | A case of gangliocytic paraganglioma in the ampulla of Vater |
title_full | A case of gangliocytic paraganglioma in the ampulla of Vater |
title_fullStr | A case of gangliocytic paraganglioma in the ampulla of Vater |
title_full_unstemmed | A case of gangliocytic paraganglioma in the ampulla of Vater |
title_short | A case of gangliocytic paraganglioma in the ampulla of Vater |
title_sort | case of gangliocytic paraganglioma in the ampulla of vater |
url | http://www.wjso.com/content/8/1/42 |
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