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Leiomyosarcoma of the portal vein: a case report and review of the literature

Leiomyosarcomas (LMS) are rare malignant tumours of smooth muscle origin predominately affecting females in their sixth decade. Only 2% of LMS arise from blood vessels and most are in the inferior vena cava. We present the first reported case of LMS of the portal vein in a male patient. Multidetecto...

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Autores principales: Chiu, Wan Hang Keith, Lo, Anthony WI, Lee, Joseph KT
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159251/
https://www.ncbi.nlm.nih.gov/pubmed/30363263
http://dx.doi.org/10.1259/bjrcr.20160125
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author Chiu, Wan Hang Keith
Lo, Anthony WI
Lee, Joseph KT
author_facet Chiu, Wan Hang Keith
Lo, Anthony WI
Lee, Joseph KT
author_sort Chiu, Wan Hang Keith
collection PubMed
description Leiomyosarcomas (LMS) are rare malignant tumours of smooth muscle origin predominately affecting females in their sixth decade. Only 2% of LMS arise from blood vessels and most are in the inferior vena cava. We present the first reported case of LMS of the portal vein in a male patient. Multidetector CT showed a large mass in the main portal vein, which was initially misinterpreted as a pancreatic cancer. Careful examination of the multidetector CT images showed radiological features of an intraluminal mass, and a preoperative diagnosis of primary LMS of the main portal vein was made. The patient underwent curative surgery and made an uneventful recovery. Awareness of this entity and recognition of the salient CT features may facilitate radiologists in making the correct preoperative diagnosis.
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spelling pubmed-61592512018-10-25 Leiomyosarcoma of the portal vein: a case report and review of the literature Chiu, Wan Hang Keith Lo, Anthony WI Lee, Joseph KT BJR Case Rep Case Report Leiomyosarcomas (LMS) are rare malignant tumours of smooth muscle origin predominately affecting females in their sixth decade. Only 2% of LMS arise from blood vessels and most are in the inferior vena cava. We present the first reported case of LMS of the portal vein in a male patient. Multidetector CT showed a large mass in the main portal vein, which was initially misinterpreted as a pancreatic cancer. Careful examination of the multidetector CT images showed radiological features of an intraluminal mass, and a preoperative diagnosis of primary LMS of the main portal vein was made. The patient underwent curative surgery and made an uneventful recovery. Awareness of this entity and recognition of the salient CT features may facilitate radiologists in making the correct preoperative diagnosis. The British Institute of Radiology 2016-12-23 /pmc/articles/PMC6159251/ /pubmed/30363263 http://dx.doi.org/10.1259/bjrcr.20160125 Text en © 2016 The Authors. Published by the British Institute of Radiology http://creativecommons.org/licenses/by/4.0/ This is an open access article 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 the original author and source are credited.
spellingShingle Case Report
Chiu, Wan Hang Keith
Lo, Anthony WI
Lee, Joseph KT
Leiomyosarcoma of the portal vein: a case report and review of the literature
title Leiomyosarcoma of the portal vein: a case report and review of the literature
title_full Leiomyosarcoma of the portal vein: a case report and review of the literature
title_fullStr Leiomyosarcoma of the portal vein: a case report and review of the literature
title_full_unstemmed Leiomyosarcoma of the portal vein: a case report and review of the literature
title_short Leiomyosarcoma of the portal vein: a case report and review of the literature
title_sort leiomyosarcoma of the portal vein: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159251/
https://www.ncbi.nlm.nih.gov/pubmed/30363263
http://dx.doi.org/10.1259/bjrcr.20160125
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