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Splenic lymphangioma in an adult

Splenic lymphangiomas are exceedingly rare benign neoplasms that occur mainly in children. They are commonly seen in the neck and axillary region. Abdominal lymphangiomas accounts for less than 5% of cases. So far, fewer than 100 cases of spleen lymphangiomas have been reported in the literature. In...

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Autores principales: Al-Shaikh, Safa A., Mubarak, Aalaa M., Harb, Zainab F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767620/
https://www.ncbi.nlm.nih.gov/pubmed/29114705
http://dx.doi.org/10.15537/smj.2017.11.20625
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author Al-Shaikh, Safa A.
Mubarak, Aalaa M.
Harb, Zainab F.
author_facet Al-Shaikh, Safa A.
Mubarak, Aalaa M.
Harb, Zainab F.
author_sort Al-Shaikh, Safa A.
collection PubMed
description Splenic lymphangiomas are exceedingly rare benign neoplasms that occur mainly in children. They are commonly seen in the neck and axillary region. Abdominal lymphangiomas accounts for less than 5% of cases. So far, fewer than 100 cases of spleen lymphangiomas have been reported in the literature. In this paper, we present one case of solitary splenic lymphangioma in a 34-year-old woman who presented with abdominal pain and weight loss for one month. The patient underwent splenectomy and diagnosis was confirmed by histopathology and immunohistochemistry studies. There was no clinical or radiological evidence of diffuse lymphangiomatosis syndrome. This case indicates that splenic lymphangiomas should be considered in the differential diagnosis of splenic cystic masses, even in adults, and should be managed with splenectomy once diagnosed to prevent complications.
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spelling pubmed-57676202018-02-06 Splenic lymphangioma in an adult Al-Shaikh, Safa A. Mubarak, Aalaa M. Harb, Zainab F. Saudi Med J Case Report Splenic lymphangiomas are exceedingly rare benign neoplasms that occur mainly in children. They are commonly seen in the neck and axillary region. Abdominal lymphangiomas accounts for less than 5% of cases. So far, fewer than 100 cases of spleen lymphangiomas have been reported in the literature. In this paper, we present one case of solitary splenic lymphangioma in a 34-year-old woman who presented with abdominal pain and weight loss for one month. The patient underwent splenectomy and diagnosis was confirmed by histopathology and immunohistochemistry studies. There was no clinical or radiological evidence of diffuse lymphangiomatosis syndrome. This case indicates that splenic lymphangiomas should be considered in the differential diagnosis of splenic cystic masses, even in adults, and should be managed with splenectomy once diagnosed to prevent complications. Saudi Medical Journal 2017-11 /pmc/articles/PMC5767620/ /pubmed/29114705 http://dx.doi.org/10.15537/smj.2017.11.20625 Text en Copyright: © Saudi Medical Journal 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
Al-Shaikh, Safa A.
Mubarak, Aalaa M.
Harb, Zainab F.
Splenic lymphangioma in an adult
title Splenic lymphangioma in an adult
title_full Splenic lymphangioma in an adult
title_fullStr Splenic lymphangioma in an adult
title_full_unstemmed Splenic lymphangioma in an adult
title_short Splenic lymphangioma in an adult
title_sort splenic lymphangioma in an adult
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767620/
https://www.ncbi.nlm.nih.gov/pubmed/29114705
http://dx.doi.org/10.15537/smj.2017.11.20625
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