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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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Autores principales: Bedir, Recep, Şehitoǧlu, İbrahim, Calapoǧlu, Ahmet Salih, Yurdakul, Cüneyt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
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.
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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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