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Spinal intradural epidermoid cyst: Case report

Spinal epidermoid cysts are rare benign tumors. The etiology can be acquired or congenital. We present a rare case of an 18-month-old girl presented 4 months ago with spontaneous intergluteal swelling fistulized to the skin and lower limbs weakness. Magnetic resonance imaging of the spine demonstrat...

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Autores principales: Elmi Saad, Moussa, El Manouni, Othmane, Boutarbouch, Mahjouba, El Ouahabi, Abdessamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199400/
https://www.ncbi.nlm.nih.gov/pubmed/37214325
http://dx.doi.org/10.1016/j.radcr.2023.04.034
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author Elmi Saad, Moussa
El Manouni, Othmane
Boutarbouch, Mahjouba
El Ouahabi, Abdessamad
author_facet Elmi Saad, Moussa
El Manouni, Othmane
Boutarbouch, Mahjouba
El Ouahabi, Abdessamad
author_sort Elmi Saad, Moussa
collection PubMed
description Spinal epidermoid cysts are rare benign tumors. The etiology can be acquired or congenital. We present a rare case of an 18-month-old girl presented 4 months ago with spontaneous intergluteal swelling fistulized to the skin and lower limbs weakness. Magnetic resonance imaging of the spine demonstrated an intradural tumor from L3 to L5 levels, isointense on T1, hyperintense on T2-weighted images with contrast enhancement after gadolinium injection without any coexistent spinal dysraphism suggested the diagnosis of the dermal sinus. The patient underwent triple-level laminectomy for biopsy and tumor resection. A pearly white tumor was encountered, with a subsequent biopsy confirming it to be an epidermoid tumor. At 6-month follow-up, the neurologic deficit was improved. Spinal epidermoid cysts are rare tumors that evolve slowly. Complete total removal is the treatment of choice.
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spelling pubmed-101994002023-05-21 Spinal intradural epidermoid cyst: Case report Elmi Saad, Moussa El Manouni, Othmane Boutarbouch, Mahjouba El Ouahabi, Abdessamad Radiol Case Rep Case Report Spinal epidermoid cysts are rare benign tumors. The etiology can be acquired or congenital. We present a rare case of an 18-month-old girl presented 4 months ago with spontaneous intergluteal swelling fistulized to the skin and lower limbs weakness. Magnetic resonance imaging of the spine demonstrated an intradural tumor from L3 to L5 levels, isointense on T1, hyperintense on T2-weighted images with contrast enhancement after gadolinium injection without any coexistent spinal dysraphism suggested the diagnosis of the dermal sinus. The patient underwent triple-level laminectomy for biopsy and tumor resection. A pearly white tumor was encountered, with a subsequent biopsy confirming it to be an epidermoid tumor. At 6-month follow-up, the neurologic deficit was improved. Spinal epidermoid cysts are rare tumors that evolve slowly. Complete total removal is the treatment of choice. Elsevier 2023-05-17 /pmc/articles/PMC10199400/ /pubmed/37214325 http://dx.doi.org/10.1016/j.radcr.2023.04.034 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Elmi Saad, Moussa
El Manouni, Othmane
Boutarbouch, Mahjouba
El Ouahabi, Abdessamad
Spinal intradural epidermoid cyst: Case report
title Spinal intradural epidermoid cyst: Case report
title_full Spinal intradural epidermoid cyst: Case report
title_fullStr Spinal intradural epidermoid cyst: Case report
title_full_unstemmed Spinal intradural epidermoid cyst: Case report
title_short Spinal intradural epidermoid cyst: Case report
title_sort spinal intradural epidermoid cyst: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199400/
https://www.ncbi.nlm.nih.gov/pubmed/37214325
http://dx.doi.org/10.1016/j.radcr.2023.04.034
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