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Solitary neurofibroma of eyelid masquerading as chalazion

Neurofibroma, a benign peripheral nerve sheath tumor, usually appears together with café-au-lait spots, iris nodules, and other tumors within the scope of neurofibromatosis von Recklinghausen type 1 tumors. A solitary neurofibroma of the eyelid is relatively rare. In this case report, we present a 3...

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Autores principales: Chen, Nancy, Hsu, Yung-Hsiang, Lee, Yuan-Chieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449116/
https://www.ncbi.nlm.nih.gov/pubmed/28579839
http://dx.doi.org/10.2147/IMCRJ.S136255
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author Chen, Nancy
Hsu, Yung-Hsiang
Lee, Yuan-Chieh
author_facet Chen, Nancy
Hsu, Yung-Hsiang
Lee, Yuan-Chieh
author_sort Chen, Nancy
collection PubMed
description Neurofibroma, a benign peripheral nerve sheath tumor, usually appears together with café-au-lait spots, iris nodules, and other tumors within the scope of neurofibromatosis von Recklinghausen type 1 tumors. A solitary neurofibroma of the eyelid is relatively rare. In this case report, we present a 39-year-old woman who had a lesion on the eyelid crease, previously treated as a chalazion. Due to persistent wound crusting, the lesion was excised above the tarsus. Pathological examination revealed a solitary neurofibroma. The patient did not have other clinical symptoms of neurofibromatosis, and there was no recurrence of the nodule during the 1-year follow-up.
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spelling pubmed-54491162017-06-02 Solitary neurofibroma of eyelid masquerading as chalazion Chen, Nancy Hsu, Yung-Hsiang Lee, Yuan-Chieh Int Med Case Rep J Case Report Neurofibroma, a benign peripheral nerve sheath tumor, usually appears together with café-au-lait spots, iris nodules, and other tumors within the scope of neurofibromatosis von Recklinghausen type 1 tumors. A solitary neurofibroma of the eyelid is relatively rare. In this case report, we present a 39-year-old woman who had a lesion on the eyelid crease, previously treated as a chalazion. Due to persistent wound crusting, the lesion was excised above the tarsus. Pathological examination revealed a solitary neurofibroma. The patient did not have other clinical symptoms of neurofibromatosis, and there was no recurrence of the nodule during the 1-year follow-up. Dove Medical Press 2017-05-23 /pmc/articles/PMC5449116/ /pubmed/28579839 http://dx.doi.org/10.2147/IMCRJ.S136255 Text en © 2017 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Chen, Nancy
Hsu, Yung-Hsiang
Lee, Yuan-Chieh
Solitary neurofibroma of eyelid masquerading as chalazion
title Solitary neurofibroma of eyelid masquerading as chalazion
title_full Solitary neurofibroma of eyelid masquerading as chalazion
title_fullStr Solitary neurofibroma of eyelid masquerading as chalazion
title_full_unstemmed Solitary neurofibroma of eyelid masquerading as chalazion
title_short Solitary neurofibroma of eyelid masquerading as chalazion
title_sort solitary neurofibroma of eyelid masquerading as chalazion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449116/
https://www.ncbi.nlm.nih.gov/pubmed/28579839
http://dx.doi.org/10.2147/IMCRJ.S136255
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