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Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease

An absence of skin lesions at the neurological onset may obscure the diagnosis of neuro-Sweet disease (NSD). We herein report a 32-year-old man with NSD in whom neurological symptoms preceded the development of skin lesions by 10 years. The patient exhibited four distinct neurological episodes: meni...

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Autores principales: Hiraga, Akiyuki, Ozaki, Daisuke, Oikawa, Makiko, Araki, Nobuyuki, Kuwabara, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928507/
https://www.ncbi.nlm.nih.gov/pubmed/31327825
http://dx.doi.org/10.2169/internalmedicine.2821-19
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author Hiraga, Akiyuki
Ozaki, Daisuke
Oikawa, Makiko
Araki, Nobuyuki
Kuwabara, Satoshi
author_facet Hiraga, Akiyuki
Ozaki, Daisuke
Oikawa, Makiko
Araki, Nobuyuki
Kuwabara, Satoshi
author_sort Hiraga, Akiyuki
collection PubMed
description An absence of skin lesions at the neurological onset may obscure the diagnosis of neuro-Sweet disease (NSD). We herein report a 32-year-old man with NSD in whom neurological symptoms preceded the development of skin lesions by 10 years. The patient exhibited four distinct neurological episodes: meningoencephalitis, scattered brain lesions, ocular flutter, and isolated seizures. Acute relapses responded to corticosteroid therapy, and the patient was successfully maintained on corticosteroid and dapsone combination therapy. NSD should be considered in the differential diagnosis of patients with recurrent neurological manifestations, especially with both meningeal and brain parenchymal involvement, even if no skin lesions are observed.
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spelling pubmed-69285072019-12-26 Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease Hiraga, Akiyuki Ozaki, Daisuke Oikawa, Makiko Araki, Nobuyuki Kuwabara, Satoshi Intern Med Case Report An absence of skin lesions at the neurological onset may obscure the diagnosis of neuro-Sweet disease (NSD). We herein report a 32-year-old man with NSD in whom neurological symptoms preceded the development of skin lesions by 10 years. The patient exhibited four distinct neurological episodes: meningoencephalitis, scattered brain lesions, ocular flutter, and isolated seizures. Acute relapses responded to corticosteroid therapy, and the patient was successfully maintained on corticosteroid and dapsone combination therapy. NSD should be considered in the differential diagnosis of patients with recurrent neurological manifestations, especially with both meningeal and brain parenchymal involvement, even if no skin lesions are observed. The Japanese Society of Internal Medicine 2019-07-22 2019-12-01 /pmc/articles/PMC6928507/ /pubmed/31327825 http://dx.doi.org/10.2169/internalmedicine.2821-19 Text en Copyright © 2019 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Hiraga, Akiyuki
Ozaki, Daisuke
Oikawa, Makiko
Araki, Nobuyuki
Kuwabara, Satoshi
Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease
title Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease
title_full Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease
title_fullStr Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease
title_full_unstemmed Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease
title_short Recurrent Neurological Episodes for 10 Years Preceding Skin Lesions in Neuro-Sweet Disease
title_sort recurrent neurological episodes for 10 years preceding skin lesions in neuro-sweet disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928507/
https://www.ncbi.nlm.nih.gov/pubmed/31327825
http://dx.doi.org/10.2169/internalmedicine.2821-19
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