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Acute onset of paraplegia due to melanocytic cervicodorsal lesion

BACKGROUND: Melanocytomas are rare pigmented tumors of the central nervous system (CNS). They are more frequent in females in their fifties and are typically benign, but locally aggressive lesions that very are rarely found in the spine. They can occur in all the age groups. CASE DESCRIPTION: A 62-y...

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Autores principales: Nigro, Raffaele, Scogna, Antonio Alessandro, Intraina, Daniele, Toccaceli, Giada, Ieraci, Alfio, Zotta, Donato Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881505/
https://www.ncbi.nlm.nih.gov/pubmed/33598337
http://dx.doi.org/10.25259/SNI_878_2020
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author Nigro, Raffaele
Scogna, Antonio Alessandro
Intraina, Daniele
Toccaceli, Giada
Ieraci, Alfio
Zotta, Donato Carlo
author_facet Nigro, Raffaele
Scogna, Antonio Alessandro
Intraina, Daniele
Toccaceli, Giada
Ieraci, Alfio
Zotta, Donato Carlo
author_sort Nigro, Raffaele
collection PubMed
description BACKGROUND: Melanocytomas are rare pigmented tumors of the central nervous system (CNS). They are more frequent in females in their fifties and are typically benign, but locally aggressive lesions that very are rarely found in the spine. They can occur in all the age groups. CASE DESCRIPTION: A 62-year-old male presented with acute paraplegia a attributed to a C7-T1 intradural extramedullary melanocytoma. Urgent surgery, consisting of subtotal removal of the lesion, resulted in subtotal recovery of motor function with full resolution of his sensory deficit. Histologically, the lesion proved to be a melanocytoma. CONCLUSION: Rarely, patients with intradural extramedullary melanocytomas of the spine may present with acute paralytic deficits warranting emergent surgical intervention.
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spelling pubmed-78815052021-02-16 Acute onset of paraplegia due to melanocytic cervicodorsal lesion Nigro, Raffaele Scogna, Antonio Alessandro Intraina, Daniele Toccaceli, Giada Ieraci, Alfio Zotta, Donato Carlo Surg Neurol Int Case Report BACKGROUND: Melanocytomas are rare pigmented tumors of the central nervous system (CNS). They are more frequent in females in their fifties and are typically benign, but locally aggressive lesions that very are rarely found in the spine. They can occur in all the age groups. CASE DESCRIPTION: A 62-year-old male presented with acute paraplegia a attributed to a C7-T1 intradural extramedullary melanocytoma. Urgent surgery, consisting of subtotal removal of the lesion, resulted in subtotal recovery of motor function with full resolution of his sensory deficit. Histologically, the lesion proved to be a melanocytoma. CONCLUSION: Rarely, patients with intradural extramedullary melanocytomas of the spine may present with acute paralytic deficits warranting emergent surgical intervention. Scientific Scholar 2021-01-20 /pmc/articles/PMC7881505/ /pubmed/33598337 http://dx.doi.org/10.25259/SNI_878_2020 Text en Copyright: © 2020 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Nigro, Raffaele
Scogna, Antonio Alessandro
Intraina, Daniele
Toccaceli, Giada
Ieraci, Alfio
Zotta, Donato Carlo
Acute onset of paraplegia due to melanocytic cervicodorsal lesion
title Acute onset of paraplegia due to melanocytic cervicodorsal lesion
title_full Acute onset of paraplegia due to melanocytic cervicodorsal lesion
title_fullStr Acute onset of paraplegia due to melanocytic cervicodorsal lesion
title_full_unstemmed Acute onset of paraplegia due to melanocytic cervicodorsal lesion
title_short Acute onset of paraplegia due to melanocytic cervicodorsal lesion
title_sort acute onset of paraplegia due to melanocytic cervicodorsal lesion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881505/
https://www.ncbi.nlm.nih.gov/pubmed/33598337
http://dx.doi.org/10.25259/SNI_878_2020
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