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A rare case of thoracic lipomyelomeningocele in a young female: A case report

Thoracic lipomyelomeningocele is a rare type of congenital occult spinal dysraphism. It is characterized by lipomatous tissue connected to the dorsal spinal cord that protrudes through a spinal defect together with the meninges or spinal cord to form a posterior mass beneath the skin. Closed spinal...

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Detalles Bibliográficos
Autores principales: Sharma, Suraj, Khadka, Hensan, Aryal, Sajiva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931526/
https://www.ncbi.nlm.nih.gov/pubmed/36819002
http://dx.doi.org/10.1016/j.radcr.2022.10.042
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author Sharma, Suraj
Khadka, Hensan
Aryal, Sajiva
author_facet Sharma, Suraj
Khadka, Hensan
Aryal, Sajiva
author_sort Sharma, Suraj
collection PubMed
description Thoracic lipomyelomeningocele is a rare type of congenital occult spinal dysraphism. It is characterized by lipomatous tissue connected to the dorsal spinal cord that protrudes through a spinal defect together with the meninges or spinal cord to form a posterior mass beneath the skin. Closed spinal dysraphism can present diagnostic challenges when resources are scarce and advanced imaging techniques like magnetic resonance imaging are not readily available. Here, we describe a case of thoracic lipomyelomeningocele, a type of closed spinal dysraphism in a young female presenting with gradually progressive weakness and tingling sensation in bilateral lower limbs over the last 6 months. On physical examination, she had a soft tissue swelling with dimpling over the dorsal spine and paraparesis. Magnetic resonance imaging of the spine revealed dorsal lipomyelomeningocele corresponding to D4-D7 vertebral levels with tethered spinal cord.
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spelling pubmed-99315262023-02-17 A rare case of thoracic lipomyelomeningocele in a young female: A case report Sharma, Suraj Khadka, Hensan Aryal, Sajiva Radiol Case Rep Case Report Thoracic lipomyelomeningocele is a rare type of congenital occult spinal dysraphism. It is characterized by lipomatous tissue connected to the dorsal spinal cord that protrudes through a spinal defect together with the meninges or spinal cord to form a posterior mass beneath the skin. Closed spinal dysraphism can present diagnostic challenges when resources are scarce and advanced imaging techniques like magnetic resonance imaging are not readily available. Here, we describe a case of thoracic lipomyelomeningocele, a type of closed spinal dysraphism in a young female presenting with gradually progressive weakness and tingling sensation in bilateral lower limbs over the last 6 months. On physical examination, she had a soft tissue swelling with dimpling over the dorsal spine and paraparesis. Magnetic resonance imaging of the spine revealed dorsal lipomyelomeningocele corresponding to D4-D7 vertebral levels with tethered spinal cord. Elsevier 2023-01-05 /pmc/articles/PMC9931526/ /pubmed/36819002 http://dx.doi.org/10.1016/j.radcr.2022.10.042 Text en © 2022 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
Sharma, Suraj
Khadka, Hensan
Aryal, Sajiva
A rare case of thoracic lipomyelomeningocele in a young female: A case report
title A rare case of thoracic lipomyelomeningocele in a young female: A case report
title_full A rare case of thoracic lipomyelomeningocele in a young female: A case report
title_fullStr A rare case of thoracic lipomyelomeningocele in a young female: A case report
title_full_unstemmed A rare case of thoracic lipomyelomeningocele in a young female: A case report
title_short A rare case of thoracic lipomyelomeningocele in a young female: A case report
title_sort rare case of thoracic lipomyelomeningocele in a young female: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931526/
https://www.ncbi.nlm.nih.gov/pubmed/36819002
http://dx.doi.org/10.1016/j.radcr.2022.10.042
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