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Presentation of massive orbital hidrocystoma at birth: case report and review of the literature

BACKGROUND: Hidrocystoma, or sudoriferous cyst, is an eyelid tumor originating from apocrine or eccrine sweat glands. Its presence in the orbit is relatively rare. CASE PRESENTATION: A full-term female child with severe right eye extrusion was referred to our department two hours after birth. We per...

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Autores principales: Eshraghi, Bahram, Abtahi, Mohammad-Ali, Sonbolastan, Seyed Ali, Kasaie, Zahra, Abtahi, Seyed-Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324226/
https://www.ncbi.nlm.nih.gov/pubmed/28251170
http://dx.doi.org/10.1186/s40662-017-0069-7
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author Eshraghi, Bahram
Abtahi, Mohammad-Ali
Sonbolastan, Seyed Ali
Kasaie, Zahra
Abtahi, Seyed-Hossein
author_facet Eshraghi, Bahram
Abtahi, Mohammad-Ali
Sonbolastan, Seyed Ali
Kasaie, Zahra
Abtahi, Seyed-Hossein
author_sort Eshraghi, Bahram
collection PubMed
description BACKGROUND: Hidrocystoma, or sudoriferous cyst, is an eyelid tumor originating from apocrine or eccrine sweat glands. Its presence in the orbit is relatively rare. CASE PRESENTATION: A full-term female child with severe right eye extrusion was referred to our department two hours after birth. We performed cyst aspiration under ultrasonic guidance; 15 cc straw-colored fluid was obtained and proptosis resolved significantly. Orbital magnetic resonance imaging (MRI) showed a large unilocular retrobulbar mass with hypo-intensity in T1 and hyper-intensity in T2. The case underwent further daily ocular assessment until day 5; when proptosis began to worsen again. On day 6, under general anesthesia, we performed aspiration and then the cyst was completely removed with an intact wall through a trans-conjunctival incision. The diameter of the aspirated cyst was about 4 cm. In pathologic consultation, a cystic cavity lined by a layer of sweat duct like epithelium with apical snouts consistent with the diagnosis of apocrine hidrocystoma was reported. CONCLUSION: To date, in the literature, six other cases of orbital hidrocystoma have been reported in childhood with protean clinical pictures; none of which presented at birth. Herein, we introduce the first case report at birth and also provide a review on the literature. Our report strongly argues against the well reputed theory of traumatic origin for orbital hidrocystoma; it has been postulated that this tumor may be the result of sweat gland cells implantation through the orbit. We thereby suggest the possible presence of choristomatous ectopic sweat gland cells in the orbit during embryogenesis.
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spelling pubmed-53242262017-03-01 Presentation of massive orbital hidrocystoma at birth: case report and review of the literature Eshraghi, Bahram Abtahi, Mohammad-Ali Sonbolastan, Seyed Ali Kasaie, Zahra Abtahi, Seyed-Hossein Eye Vis (Lond) Case Report BACKGROUND: Hidrocystoma, or sudoriferous cyst, is an eyelid tumor originating from apocrine or eccrine sweat glands. Its presence in the orbit is relatively rare. CASE PRESENTATION: A full-term female child with severe right eye extrusion was referred to our department two hours after birth. We performed cyst aspiration under ultrasonic guidance; 15 cc straw-colored fluid was obtained and proptosis resolved significantly. Orbital magnetic resonance imaging (MRI) showed a large unilocular retrobulbar mass with hypo-intensity in T1 and hyper-intensity in T2. The case underwent further daily ocular assessment until day 5; when proptosis began to worsen again. On day 6, under general anesthesia, we performed aspiration and then the cyst was completely removed with an intact wall through a trans-conjunctival incision. The diameter of the aspirated cyst was about 4 cm. In pathologic consultation, a cystic cavity lined by a layer of sweat duct like epithelium with apical snouts consistent with the diagnosis of apocrine hidrocystoma was reported. CONCLUSION: To date, in the literature, six other cases of orbital hidrocystoma have been reported in childhood with protean clinical pictures; none of which presented at birth. Herein, we introduce the first case report at birth and also provide a review on the literature. Our report strongly argues against the well reputed theory of traumatic origin for orbital hidrocystoma; it has been postulated that this tumor may be the result of sweat gland cells implantation through the orbit. We thereby suggest the possible presence of choristomatous ectopic sweat gland cells in the orbit during embryogenesis. BioMed Central 2017-02-23 /pmc/articles/PMC5324226/ /pubmed/28251170 http://dx.doi.org/10.1186/s40662-017-0069-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Eshraghi, Bahram
Abtahi, Mohammad-Ali
Sonbolastan, Seyed Ali
Kasaie, Zahra
Abtahi, Seyed-Hossein
Presentation of massive orbital hidrocystoma at birth: case report and review of the literature
title Presentation of massive orbital hidrocystoma at birth: case report and review of the literature
title_full Presentation of massive orbital hidrocystoma at birth: case report and review of the literature
title_fullStr Presentation of massive orbital hidrocystoma at birth: case report and review of the literature
title_full_unstemmed Presentation of massive orbital hidrocystoma at birth: case report and review of the literature
title_short Presentation of massive orbital hidrocystoma at birth: case report and review of the literature
title_sort presentation of massive orbital hidrocystoma at birth: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324226/
https://www.ncbi.nlm.nih.gov/pubmed/28251170
http://dx.doi.org/10.1186/s40662-017-0069-7
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