Epidermoid cyst of spleen mimicking splenic lymphangioma

Primary splenic cyst is a relatively rare entity; they comprise only about 10% of benign non-parasitic cysts. Most of these are asymptomatic and are observed incidentally during abdominal ultrasonography. The number of diagnosed splenic cyst cases seems to have risen because of the increasing use of...

Full description

Bibliographic Details
Main Authors: Garg, Monika, Kataria, Sant P., Sethi, Divya, Mathur, Satyavir Kumar
Format: Online
Language:English
Published: Medknow Publications & Media Pvt Ltd 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905332/
id pubmed-3905332
recordtype oai_dc
spelling pubmed-39053322014-02-10 Epidermoid cyst of spleen mimicking splenic lymphangioma Garg, Monika Kataria, Sant P. Sethi, Divya Mathur, Satyavir Kumar Case Report Primary splenic cyst is a relatively rare entity; they comprise only about 10% of benign non-parasitic cysts. Most of these are asymptomatic and are observed incidentally during abdominal ultrasonography. The number of diagnosed splenic cyst cases seems to have risen because of the increasing use of abdominal imaging techniques. However, definite diagnosis is possible only after splenectomy when epithelial lining is confirmed histologically. We report a case of a 14-year-old child who presented with fullness of abdomen and pain in the left hypochondrium since last few months. First impression made was in favor of a splenic lymphangioma of size 8 × 8 cm which was based on a Computerized tomography scan and the sonographic findings. Splenectomy was performed and was sent for histopathological examination which in combination with immunohistochemistry revealed findings suggestive of primary epithelial cyst. A large cystic mass with a relatively thin wall localized in the spleen is likely to be a primary or secondary cyst. The diagnosis of false cyst should be favored if there is a clear history of trauma, if the patient is older than fourth decade, if there is a hematoma elsewhere in spleen, or if cyst wall is calcified. This rare entity should be considered in the differential diagnosis in a patient presenting with left hypochondrial pain. Medknow Publications & Media Pvt Ltd 2013-06-29 /pmc/articles/PMC3905332/ /pubmed/24516849 http://dx.doi.org/10.4103/2277-9175.114190 Text en Copyright: © 2013 Garg. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Garg, Monika
Kataria, Sant P.
Sethi, Divya
Mathur, Satyavir Kumar
spellingShingle Garg, Monika
Kataria, Sant P.
Sethi, Divya
Mathur, Satyavir Kumar
Epidermoid cyst of spleen mimicking splenic lymphangioma
author_facet Garg, Monika
Kataria, Sant P.
Sethi, Divya
Mathur, Satyavir Kumar
author_sort Garg, Monika
title Epidermoid cyst of spleen mimicking splenic lymphangioma
title_short Epidermoid cyst of spleen mimicking splenic lymphangioma
title_full Epidermoid cyst of spleen mimicking splenic lymphangioma
title_fullStr Epidermoid cyst of spleen mimicking splenic lymphangioma
title_full_unstemmed Epidermoid cyst of spleen mimicking splenic lymphangioma
title_sort epidermoid cyst of spleen mimicking splenic lymphangioma
description Primary splenic cyst is a relatively rare entity; they comprise only about 10% of benign non-parasitic cysts. Most of these are asymptomatic and are observed incidentally during abdominal ultrasonography. The number of diagnosed splenic cyst cases seems to have risen because of the increasing use of abdominal imaging techniques. However, definite diagnosis is possible only after splenectomy when epithelial lining is confirmed histologically. We report a case of a 14-year-old child who presented with fullness of abdomen and pain in the left hypochondrium since last few months. First impression made was in favor of a splenic lymphangioma of size 8 × 8 cm which was based on a Computerized tomography scan and the sonographic findings. Splenectomy was performed and was sent for histopathological examination which in combination with immunohistochemistry revealed findings suggestive of primary epithelial cyst. A large cystic mass with a relatively thin wall localized in the spleen is likely to be a primary or secondary cyst. The diagnosis of false cyst should be favored if there is a clear history of trauma, if the patient is older than fourth decade, if there is a hematoma elsewhere in spleen, or if cyst wall is calcified. This rare entity should be considered in the differential diagnosis in a patient presenting with left hypochondrial pain.
publisher Medknow Publications & Media Pvt Ltd
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905332/
_version_ 1612052285062381568