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Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype

Neurocutaneous melanosis (NCM) is a rare congenital disorder. Most of the cases described in literature for this entity have involvement of the leptomeninges and other structures of brain such as brain stem, temporal lobes, and spinal meninges and no involvement of leptomeninges and presence of lesi...

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Autores principales: Kumar, Sanjay, Dey, Subir, Pimpalwar, Yayati, Rao, Akhilesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144608/
https://www.ncbi.nlm.nih.gov/pubmed/30271467
http://dx.doi.org/10.4103/JPN.JPN_53_18
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author Kumar, Sanjay
Dey, Subir
Pimpalwar, Yayati
Rao, Akhilesh
author_facet Kumar, Sanjay
Dey, Subir
Pimpalwar, Yayati
Rao, Akhilesh
author_sort Kumar, Sanjay
collection PubMed
description Neurocutaneous melanosis (NCM) is a rare congenital disorder. Most of the cases described in literature for this entity have involvement of the leptomeninges and other structures of brain such as brain stem, temporal lobes, and spinal meninges and no involvement of leptomeninges and presence of lesions in bilateral temporal lobes. NCM without the involvement of leptomeninges should be considered a distinct entity as the prognosis is favorable as compared to cases with leptomeningeal involvement who develop early hydrocephalus and multiple cranial nerve palsies.
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spelling pubmed-61446082018-09-28 Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype Kumar, Sanjay Dey, Subir Pimpalwar, Yayati Rao, Akhilesh J Pediatr Neurosci Neuroimaging Neurocutaneous melanosis (NCM) is a rare congenital disorder. Most of the cases described in literature for this entity have involvement of the leptomeninges and other structures of brain such as brain stem, temporal lobes, and spinal meninges and no involvement of leptomeninges and presence of lesions in bilateral temporal lobes. NCM without the involvement of leptomeninges should be considered a distinct entity as the prognosis is favorable as compared to cases with leptomeningeal involvement who develop early hydrocephalus and multiple cranial nerve palsies. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6144608/ /pubmed/30271467 http://dx.doi.org/10.4103/JPN.JPN_53_18 Text en Copyright: © 2018 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Neuroimaging
Kumar, Sanjay
Dey, Subir
Pimpalwar, Yayati
Rao, Akhilesh
Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype
title Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype
title_full Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype
title_fullStr Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype
title_full_unstemmed Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype
title_short Neurocutaneous Melanosis with Bilateral Temporal Lobe Lesions without Leptomeningeal Enhancement: A Distinct Entity or Subtype
title_sort neurocutaneous melanosis with bilateral temporal lobe lesions without leptomeningeal enhancement: a distinct entity or subtype
topic Neuroimaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144608/
https://www.ncbi.nlm.nih.gov/pubmed/30271467
http://dx.doi.org/10.4103/JPN.JPN_53_18
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