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Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report
Solid hamartoma of the pancreas is very rare, and only 3 cases have been reported thus far. A patient underwent pancreaticoduodenectomy due to a mass in the head of the pancreas which was suspected to be a borderline malignant tumor, but the histologic diagnosis turned out to be myoepithelial hamart...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Association of Hepato-Biliary-Pancreatic Surgery
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574988/ https://www.ncbi.nlm.nih.gov/pubmed/26388912 http://dx.doi.org/10.14701/kjhbps.2012.16.2.80 |
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author | Kwon, Wooil Kim, Sun-Whe Lee, Kyoung Bun Jang, Jin-Young Park, Jae Woo Han, In Woong Kang, Mee Joo |
author_facet | Kwon, Wooil Kim, Sun-Whe Lee, Kyoung Bun Jang, Jin-Young Park, Jae Woo Han, In Woong Kang, Mee Joo |
author_sort | Kwon, Wooil |
collection | PubMed |
description | Solid hamartoma of the pancreas is very rare, and only 3 cases have been reported thus far. A patient underwent pancreaticoduodenectomy due to a mass in the head of the pancreas which was suspected to be a borderline malignant tumor, but the histologic diagnosis turned out to be myoepithelial hamartoma (MEH) or adenomyoma. It was characterized by benign duct and glandular structures surrounded by proliferating smooth muscle, and acinus formation was not observed. Immunohistochemical stain for smooth muscle actin (SMA) was positive in spindle cells, and CD34 was negative, differentiating it from the three previously reported cases of solid hamartoma of the pancreas. MEH is an entity that is on the same spectrum as heterotopic pancreas. MEH is rare and has usually been reported in the gastrointestinal tract. To the best of our knowledge, MEH has never been reported in the pancreas. Therefore we report the world's first documented case of MEH of the pancreas. |
format | Online Article Text |
id | pubmed-4574988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean Association of Hepato-Biliary-Pancreatic Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-45749882015-09-18 Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report Kwon, Wooil Kim, Sun-Whe Lee, Kyoung Bun Jang, Jin-Young Park, Jae Woo Han, In Woong Kang, Mee Joo Korean J Hepatobiliary Pancreat Surg Case Report Solid hamartoma of the pancreas is very rare, and only 3 cases have been reported thus far. A patient underwent pancreaticoduodenectomy due to a mass in the head of the pancreas which was suspected to be a borderline malignant tumor, but the histologic diagnosis turned out to be myoepithelial hamartoma (MEH) or adenomyoma. It was characterized by benign duct and glandular structures surrounded by proliferating smooth muscle, and acinus formation was not observed. Immunohistochemical stain for smooth muscle actin (SMA) was positive in spindle cells, and CD34 was negative, differentiating it from the three previously reported cases of solid hamartoma of the pancreas. MEH is an entity that is on the same spectrum as heterotopic pancreas. MEH is rare and has usually been reported in the gastrointestinal tract. To the best of our knowledge, MEH has never been reported in the pancreas. Therefore we report the world's first documented case of MEH of the pancreas. Korean Association of Hepato-Biliary-Pancreatic Surgery 2012-05 2012-05-31 /pmc/articles/PMC4574988/ /pubmed/26388912 http://dx.doi.org/10.14701/kjhbps.2012.16.2.80 Text en Copyright © 2012 by The Korean Association of Hepato-Biliary-Pancreatic Surgery http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kwon, Wooil Kim, Sun-Whe Lee, Kyoung Bun Jang, Jin-Young Park, Jae Woo Han, In Woong Kang, Mee Joo Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
title | Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
title_full | Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
title_fullStr | Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
title_full_unstemmed | Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
title_short | Myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
title_sort | myoepithelial hamartoma as a solitary mass in the pancreatic parenchyma: the first case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574988/ https://www.ncbi.nlm.nih.gov/pubmed/26388912 http://dx.doi.org/10.14701/kjhbps.2012.16.2.80 |
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