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Portal vein leiomyosarcoma: a case report and review of the literature

BACKGROUND: Leiomyosarcoma of vascular smooth muscle is a very rare entity. A fair number of cases of vascular leiomyosarcomas have been reported, and the vast majority of these tumors arose from the inferior vena cava. CASE PRESENTATION: We report the case of a 71-year-old female patient who presen...

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Autores principales: Gohrbandt, Antje E., Hansen, Torsten, Ell, Christian, Heinrich, Stefan S., Lang, Hauke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007823/
https://www.ncbi.nlm.nih.gov/pubmed/27580598
http://dx.doi.org/10.1186/s12893-016-0174-x
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author Gohrbandt, Antje E.
Hansen, Torsten
Ell, Christian
Heinrich, Stefan S.
Lang, Hauke
author_facet Gohrbandt, Antje E.
Hansen, Torsten
Ell, Christian
Heinrich, Stefan S.
Lang, Hauke
author_sort Gohrbandt, Antje E.
collection PubMed
description BACKGROUND: Leiomyosarcoma of vascular smooth muscle is a very rare entity. A fair number of cases of vascular leiomyosarcomas have been reported, and the vast majority of these tumors arose from the inferior vena cava. CASE PRESENTATION: We report the case of a 71-year-old female patient who presented with recurrent upper abdominal pain. A CT-scan demonstrated a heterogenous mass in the liver hilum. Liver function tests and hematology parameters as well as the tumor markers were normal. Due to the unclear diagnosis a percutaneous biopsy of this mass was performed and revealed leiomyosarcoma. The patient was treated by a right sided hemihepatectomy with portal vein reconstruction and an end-to-side hepatico-jejunostomy. Final histology confirmed complete (R0) resection of a moderately differentiated leiomyosarcoma of the portal vein. After complete (R0) resection of the lesion, the patient remained without any signs of tumor recurrence for a total of 36 months until detection of an unresectable local recurrence. After surgical re-exploration the patient was finally referred to palliative radiotherapy. CONCLUSION: Vascular leiomyosarcoma of the portal vein is an extremely rare tumor entity. We have described a case with no evidence-based neo/adjuvant treatment options, where aggressive surgery achieved a tumor-free margin (R0), performed in a specialized center for sarcoma and hepatobiliary surgery.
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spelling pubmed-50078232016-09-02 Portal vein leiomyosarcoma: a case report and review of the literature Gohrbandt, Antje E. Hansen, Torsten Ell, Christian Heinrich, Stefan S. Lang, Hauke BMC Surg Case Report BACKGROUND: Leiomyosarcoma of vascular smooth muscle is a very rare entity. A fair number of cases of vascular leiomyosarcomas have been reported, and the vast majority of these tumors arose from the inferior vena cava. CASE PRESENTATION: We report the case of a 71-year-old female patient who presented with recurrent upper abdominal pain. A CT-scan demonstrated a heterogenous mass in the liver hilum. Liver function tests and hematology parameters as well as the tumor markers were normal. Due to the unclear diagnosis a percutaneous biopsy of this mass was performed and revealed leiomyosarcoma. The patient was treated by a right sided hemihepatectomy with portal vein reconstruction and an end-to-side hepatico-jejunostomy. Final histology confirmed complete (R0) resection of a moderately differentiated leiomyosarcoma of the portal vein. After complete (R0) resection of the lesion, the patient remained without any signs of tumor recurrence for a total of 36 months until detection of an unresectable local recurrence. After surgical re-exploration the patient was finally referred to palliative radiotherapy. CONCLUSION: Vascular leiomyosarcoma of the portal vein is an extremely rare tumor entity. We have described a case with no evidence-based neo/adjuvant treatment options, where aggressive surgery achieved a tumor-free margin (R0), performed in a specialized center for sarcoma and hepatobiliary surgery. BioMed Central 2016-09-01 /pmc/articles/PMC5007823/ /pubmed/27580598 http://dx.doi.org/10.1186/s12893-016-0174-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Gohrbandt, Antje E.
Hansen, Torsten
Ell, Christian
Heinrich, Stefan S.
Lang, Hauke
Portal vein leiomyosarcoma: a case report and review of the literature
title Portal vein leiomyosarcoma: a case report and review of the literature
title_full Portal vein leiomyosarcoma: a case report and review of the literature
title_fullStr Portal vein leiomyosarcoma: a case report and review of the literature
title_full_unstemmed Portal vein leiomyosarcoma: a case report and review of the literature
title_short Portal vein leiomyosarcoma: a case report and review of the literature
title_sort portal vein leiomyosarcoma: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007823/
https://www.ncbi.nlm.nih.gov/pubmed/27580598
http://dx.doi.org/10.1186/s12893-016-0174-x
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AT heinrichstefans portalveinleiomyosarcomaacasereportandreviewoftheliterature
AT langhauke portalveinleiomyosarcomaacasereportandreviewoftheliterature