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A Rare Case of Splenic Littoral Cell Angioma in a Child
Littoral cell angioma (LCA) is a rare, benign primary vascular neoplasm of the spleen. The tumor originates from the littoral cells lining the sinuses of the red pulp of the spleen. Preoperative distinction of this tumor from other benign or malign splenic lesions is difficult. Radiologically most c...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196359/ https://www.ncbi.nlm.nih.gov/pubmed/25328338 http://dx.doi.org/10.4103/0974-2727.141511 |
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author | Bedir, Recep Şehitoǧlu, İbrahim Calapoǧlu, Ahmet Salih Yurdakul, Cüneyt |
author_facet | Bedir, Recep Şehitoǧlu, İbrahim Calapoǧlu, Ahmet Salih Yurdakul, Cüneyt |
author_sort | Bedir, Recep |
collection | PubMed |
description | Littoral cell angioma (LCA) is a rare, benign primary vascular neoplasm of the spleen. The tumor originates from the littoral cells lining the sinuses of the red pulp of the spleen. Preoperative distinction of this tumor from other benign or malign splenic lesions is difficult. Radiologically most cases present as multiple nodules. Definitive diagnosis can only be made histopathologically and immunohistochemically following splenectomy. This clinical situation can coexist with various malignancies and autoimmune disorders. Even though, it is mostly benign, since it has the potential to become malignant after splenectomy, long-term follow-up is required. We present an LCA case, which appeared as a solitary mass in the spleen of an 11-year-old girl with abdominal pain admitted to our hospital. |
format | Online Article Text |
id | pubmed-4196359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41963592014-10-17 A Rare Case of Splenic Littoral Cell Angioma in a Child Bedir, Recep Şehitoǧlu, İbrahim Calapoǧlu, Ahmet Salih Yurdakul, Cüneyt J Lab Physicians Case Report Littoral cell angioma (LCA) is a rare, benign primary vascular neoplasm of the spleen. The tumor originates from the littoral cells lining the sinuses of the red pulp of the spleen. Preoperative distinction of this tumor from other benign or malign splenic lesions is difficult. Radiologically most cases present as multiple nodules. Definitive diagnosis can only be made histopathologically and immunohistochemically following splenectomy. This clinical situation can coexist with various malignancies and autoimmune disorders. Even though, it is mostly benign, since it has the potential to become malignant after splenectomy, long-term follow-up is required. We present an LCA case, which appeared as a solitary mass in the spleen of an 11-year-old girl with abdominal pain admitted to our hospital. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4196359/ /pubmed/25328338 http://dx.doi.org/10.4103/0974-2727.141511 Text en Copyright: © Journal of Laboratory Physicians http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bedir, Recep Şehitoǧlu, İbrahim Calapoǧlu, Ahmet Salih Yurdakul, Cüneyt A Rare Case of Splenic Littoral Cell Angioma in a Child |
title | A Rare Case of Splenic Littoral Cell Angioma in a Child |
title_full | A Rare Case of Splenic Littoral Cell Angioma in a Child |
title_fullStr | A Rare Case of Splenic Littoral Cell Angioma in a Child |
title_full_unstemmed | A Rare Case of Splenic Littoral Cell Angioma in a Child |
title_short | A Rare Case of Splenic Littoral Cell Angioma in a Child |
title_sort | rare case of splenic littoral cell angioma in a child |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196359/ https://www.ncbi.nlm.nih.gov/pubmed/25328338 http://dx.doi.org/10.4103/0974-2727.141511 |
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