Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report

Undifferentiated connective tissue disease (UCTD) represents a group of diseases which do not fulfill the criteria of rheumatologic diseases or may be considered as an early stage of any of these diseases. Axial spondyloarthritis (axSpA) is a disease accompanied by symptoms of inflammatory low back...

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Autores principales: Mansız-Kaplan, Başak, Nacır, Barış, Mülkoğlu, Cevriye, Pervane-Vural, Seçil, Genç, Hakan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bayçınar Medical Publishing 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088801/
https://www.ncbi.nlm.nih.gov/pubmed/33948552
http://dx.doi.org/10.5606/tftrd.2021.4909
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author Mansız-Kaplan, Başak
Nacır, Barış
Mülkoğlu, Cevriye
Pervane-Vural, Seçil
Genç, Hakan
author_facet Mansız-Kaplan, Başak
Nacır, Barış
Mülkoğlu, Cevriye
Pervane-Vural, Seçil
Genç, Hakan
author_sort Mansız-Kaplan, Başak
collection PubMed
description Undifferentiated connective tissue disease (UCTD) represents a group of diseases which do not fulfill the criteria of rheumatologic diseases or may be considered as an early stage of any of these diseases. Axial spondyloarthritis (axSpA) is a disease accompanied by symptoms of inflammatory low back pain and peripheral symptoms, with more spine and sacroiliac joint involvement. In this report, we, for the first time, present a case of UCTD presenting with axSpA in whom the initial finding was optic neuritis, which is rarely seen in UCTD.
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spelling pubmed-80888012021-05-03 Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report Mansız-Kaplan, Başak Nacır, Barış Mülkoğlu, Cevriye Pervane-Vural, Seçil Genç, Hakan Turk J Phys Med Rehabil Case Report Undifferentiated connective tissue disease (UCTD) represents a group of diseases which do not fulfill the criteria of rheumatologic diseases or may be considered as an early stage of any of these diseases. Axial spondyloarthritis (axSpA) is a disease accompanied by symptoms of inflammatory low back pain and peripheral symptoms, with more spine and sacroiliac joint involvement. In this report, we, for the first time, present a case of UCTD presenting with axSpA in whom the initial finding was optic neuritis, which is rarely seen in UCTD. Bayçınar Medical Publishing 2021-03-04 /pmc/articles/PMC8088801/ /pubmed/33948552 http://dx.doi.org/10.5606/tftrd.2021.4909 Text en Copyright © 2021, Turkish Society of Physical Medicine and Rehabilitation https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Report
Mansız-Kaplan, Başak
Nacır, Barış
Mülkoğlu, Cevriye
Pervane-Vural, Seçil
Genç, Hakan
Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report
title Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report
title_full Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report
title_fullStr Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report
title_full_unstemmed Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report
title_short Undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: A rare case report
title_sort undifferentiated connective tissue disease presenting with optic neuritis and concomitant axial spondyloarthritis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088801/
https://www.ncbi.nlm.nih.gov/pubmed/33948552
http://dx.doi.org/10.5606/tftrd.2021.4909
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