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Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy

Relapsing polychondritis (RP) is a rare autoimmune disease that is characterized by inflammatory reaction of unknown etiology and destruction of cartilaginous structures. Characteristic symptoms of this disease include cartilage inflammation of the ear, nose, larynx, trachea, bronchi, joints, eyes,...

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Autores principales: Ahn, Suk-Won, Park, Moo-Seok, Jeong, Hae-Bong, Kwon, Oh-Sang, Yoon, Byung-Nam, Kim, Hee Sung, Choi, Sang Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326716/
https://www.ncbi.nlm.nih.gov/pubmed/28243168
http://dx.doi.org/10.5607/en.2017.26.1.66
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author Ahn, Suk-Won
Park, Moo-Seok
Jeong, Hae-Bong
Kwon, Oh-Sang
Yoon, Byung-Nam
Kim, Hee Sung
Choi, Sang Tae
author_facet Ahn, Suk-Won
Park, Moo-Seok
Jeong, Hae-Bong
Kwon, Oh-Sang
Yoon, Byung-Nam
Kim, Hee Sung
Choi, Sang Tae
author_sort Ahn, Suk-Won
collection PubMed
description Relapsing polychondritis (RP) is a rare autoimmune disease that is characterized by inflammatory reaction of unknown etiology and destruction of cartilaginous structures. Characteristic symptoms of this disease include cartilage inflammation of the ear, nose, larynx, trachea, bronchi, joints, eyes, heart and skin. Concomitance with neurologic symptom is very rare in RP, and the detailed underlying mechanism of neurological involvement associated with RP is not fully understood. We herein described an unusual recurrent case of inflammatory brain lesions associated with RP, with attention to clinical manifestations, autoimmune disease involvement, and therapeutic effects.
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spelling pubmed-53267162017-02-27 Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy Ahn, Suk-Won Park, Moo-Seok Jeong, Hae-Bong Kwon, Oh-Sang Yoon, Byung-Nam Kim, Hee Sung Choi, Sang Tae Exp Neurobiol Case Report Relapsing polychondritis (RP) is a rare autoimmune disease that is characterized by inflammatory reaction of unknown etiology and destruction of cartilaginous structures. Characteristic symptoms of this disease include cartilage inflammation of the ear, nose, larynx, trachea, bronchi, joints, eyes, heart and skin. Concomitance with neurologic symptom is very rare in RP, and the detailed underlying mechanism of neurological involvement associated with RP is not fully understood. We herein described an unusual recurrent case of inflammatory brain lesions associated with RP, with attention to clinical manifestations, autoimmune disease involvement, and therapeutic effects. The Korean Society for Brain and Neural Science 2017-02 2016-12-21 /pmc/articles/PMC5326716/ /pubmed/28243168 http://dx.doi.org/10.5607/en.2017.26.1.66 Text en Copyright © Experimental Neurobiology 2017. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ahn, Suk-Won
Park, Moo-Seok
Jeong, Hae-Bong
Kwon, Oh-Sang
Yoon, Byung-Nam
Kim, Hee Sung
Choi, Sang Tae
Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
title Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
title_full Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
title_fullStr Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
title_full_unstemmed Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
title_short Relapsing Polychondritis Presented with Encephalitis Followed by Brain Atrophy
title_sort relapsing polychondritis presented with encephalitis followed by brain atrophy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326716/
https://www.ncbi.nlm.nih.gov/pubmed/28243168
http://dx.doi.org/10.5607/en.2017.26.1.66
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