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Splenic Angiosarcoma: A Diagnostic Splenectomy Finding

Splenic tumors are not frequent. Blood vessel neoplasms are a rare category of tumors and have an extremely low incidence in the spleen. This case report aims to describe a 57-year-old woman in whom a routine imaging examination had shown splenic cysts. During her follow-up, the cysts became larger...

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Detalles Bibliográficos
Autores principales: de Azevedo, Otavio Schmidt, do Nascimento Santos, Bruna, de Souza Liboni, Nelson, da Costa, Juliano Fernandes, de Campos, Olimpio Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126591/
https://www.ncbi.nlm.nih.gov/pubmed/27920710
http://dx.doi.org/10.1159/000452619
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author de Azevedo, Otavio Schmidt
do Nascimento Santos, Bruna
de Souza Liboni, Nelson
da Costa, Juliano Fernandes
de Campos, Olimpio Daniel
author_facet de Azevedo, Otavio Schmidt
do Nascimento Santos, Bruna
de Souza Liboni, Nelson
da Costa, Juliano Fernandes
de Campos, Olimpio Daniel
author_sort de Azevedo, Otavio Schmidt
collection PubMed
description Splenic tumors are not frequent. Blood vessel neoplasms are a rare category of tumors and have an extremely low incidence in the spleen. This case report aims to describe a 57-year-old woman in whom a routine imaging examination had shown splenic cysts. During her follow-up, the cysts became larger and increased in number. A diagnostic splenectomy was performed and its analysis showed a rare splenic angiosarcoma.
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spelling pubmed-51265912016-12-05 Splenic Angiosarcoma: A Diagnostic Splenectomy Finding de Azevedo, Otavio Schmidt do Nascimento Santos, Bruna de Souza Liboni, Nelson da Costa, Juliano Fernandes de Campos, Olimpio Daniel Case Rep Oncol Case Report Splenic tumors are not frequent. Blood vessel neoplasms are a rare category of tumors and have an extremely low incidence in the spleen. This case report aims to describe a 57-year-old woman in whom a routine imaging examination had shown splenic cysts. During her follow-up, the cysts became larger and increased in number. A diagnostic splenectomy was performed and its analysis showed a rare splenic angiosarcoma. S. Karger AG 2016-11-14 /pmc/articles/PMC5126591/ /pubmed/27920710 http://dx.doi.org/10.1159/000452619 Text en Copyright © 2016 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
de Azevedo, Otavio Schmidt
do Nascimento Santos, Bruna
de Souza Liboni, Nelson
da Costa, Juliano Fernandes
de Campos, Olimpio Daniel
Splenic Angiosarcoma: A Diagnostic Splenectomy Finding
title Splenic Angiosarcoma: A Diagnostic Splenectomy Finding
title_full Splenic Angiosarcoma: A Diagnostic Splenectomy Finding
title_fullStr Splenic Angiosarcoma: A Diagnostic Splenectomy Finding
title_full_unstemmed Splenic Angiosarcoma: A Diagnostic Splenectomy Finding
title_short Splenic Angiosarcoma: A Diagnostic Splenectomy Finding
title_sort splenic angiosarcoma: a diagnostic splenectomy finding
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126591/
https://www.ncbi.nlm.nih.gov/pubmed/27920710
http://dx.doi.org/10.1159/000452619
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