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Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection
Primary hepatic leiomyosarcoma (PHL) is an extremely rare tumor. The tumor has no specific presentations and often diagnosis is delayed until it reaches a significant size. We report the case of a 69-year-old female presented with a huge PHL. Due to size of the tumor and to be operable, the patient...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association of Hepato-Biliary-Pancreatic Surgery
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736744/ https://www.ncbi.nlm.nih.gov/pubmed/29264587 http://dx.doi.org/10.14701/ahbps.2017.21.4.228 |
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author | Giakoustidis, Dimitrios Giakoustidis, Alexander Goulopoulos, Thomas Arabatzi, Ntina Kainantidis, Aristidis Zaraboukas, Thomas |
author_facet | Giakoustidis, Dimitrios Giakoustidis, Alexander Goulopoulos, Thomas Arabatzi, Ntina Kainantidis, Aristidis Zaraboukas, Thomas |
author_sort | Giakoustidis, Dimitrios |
collection | PubMed |
description | Primary hepatic leiomyosarcoma (PHL) is an extremely rare tumor. The tumor has no specific presentations and often diagnosis is delayed until it reaches a significant size. We report the case of a 69-year-old female presented with a huge PHL. Due to size of the tumor and to be operable, the patient subjected to right portal vein embolization (PVE) and selective embolization of segment V. Four weeks after the PVE, liver resection was conducted (Segments V+VI bisegmentectomy plus resection of IVA). The patient had an uncomplicated post-operative course, and discharged at the 8th post-operative day. Diagnosis of PHL was confirmed by histopathological and immunohistochemical examinations. The patient refused to receive adjuvant chemotherapy, and revealed evidence of recurrence six months after the operation, and finally died 12 months after the operation and 16 months after initial diagnosis. PHL is an extremely rare tumor and often in first presentation has significant size. Radical surgery with adjuvant chemotherapy is key feature for prolonged survival. |
format | Online Article Text |
id | pubmed-5736744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Association of Hepato-Biliary-Pancreatic Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-57367442017-12-20 Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection Giakoustidis, Dimitrios Giakoustidis, Alexander Goulopoulos, Thomas Arabatzi, Ntina Kainantidis, Aristidis Zaraboukas, Thomas Ann Hepatobiliary Pancreat Surg Case Report Primary hepatic leiomyosarcoma (PHL) is an extremely rare tumor. The tumor has no specific presentations and often diagnosis is delayed until it reaches a significant size. We report the case of a 69-year-old female presented with a huge PHL. Due to size of the tumor and to be operable, the patient subjected to right portal vein embolization (PVE) and selective embolization of segment V. Four weeks after the PVE, liver resection was conducted (Segments V+VI bisegmentectomy plus resection of IVA). The patient had an uncomplicated post-operative course, and discharged at the 8th post-operative day. Diagnosis of PHL was confirmed by histopathological and immunohistochemical examinations. The patient refused to receive adjuvant chemotherapy, and revealed evidence of recurrence six months after the operation, and finally died 12 months after the operation and 16 months after initial diagnosis. PHL is an extremely rare tumor and often in first presentation has significant size. Radical surgery with adjuvant chemotherapy is key feature for prolonged survival. Korean Association of Hepato-Biliary-Pancreatic Surgery 2017-11 2017-11-30 /pmc/articles/PMC5736744/ /pubmed/29264587 http://dx.doi.org/10.14701/ahbps.2017.21.4.228 Text en Copyright © 2017 by The Korean Association of Hepato-Biliary-Pancreatic Surgery http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Giakoustidis, Dimitrios Giakoustidis, Alexander Goulopoulos, Thomas Arabatzi, Ntina Kainantidis, Aristidis Zaraboukas, Thomas Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
title | Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
title_full | Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
title_fullStr | Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
title_full_unstemmed | Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
title_short | Primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
title_sort | primary gigantic leiomyosarcoma of the liver treated with portal vein embolization and liver resection |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736744/ https://www.ncbi.nlm.nih.gov/pubmed/29264587 http://dx.doi.org/10.14701/ahbps.2017.21.4.228 |
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