Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody

Neuromyelitis Optic (NMO) is an inflammatory disorder involving central nervous system which often co-exists with other autoimmune diseases such as Sjögren’s syndrome (SS). NMO manifestation could precede or follow SS, but the role of anti-SSA in the pathogenesis of NMO remains unclear. We present a...

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Main Authors: Riwanti Estiasari, Salsabila Firdausia, Dewi Wulandari, Kartika Maharani, Freddy Sitorus, David Pangeran, Darma Imran
Format: Article
Language:English
Published: MDPI AG 2019-03-01
Series:Neurology International
Subjects:
Online Access:https://pagepress.org/journals/index.php/ni/article/view/7958
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author Riwanti Estiasari
Salsabila Firdausia
Dewi Wulandari
Kartika Maharani
Freddy Sitorus
David Pangeran
Darma Imran
author_facet Riwanti Estiasari
Salsabila Firdausia
Dewi Wulandari
Kartika Maharani
Freddy Sitorus
David Pangeran
Darma Imran
author_sort Riwanti Estiasari
collection DOAJ
description Neuromyelitis Optic (NMO) is an inflammatory disorder involving central nervous system which often co-exists with other autoimmune diseases such as Sjögren’s syndrome (SS). NMO manifestation could precede or follow SS, but the role of anti-SSA in the pathogenesis of NMO remains unclear. We present a case of NMO with anti-AQP4 anti-SSA antibody positive. A-44-year-old female presented with right side weakness. The symptoms began with numbness that improved spontaneously. She also complained pain and dry sensations on her eyes. Schirmer test on her left eye, antinuclear antibody (ANA) and anti- SSA antibody were positive. Cervical MRI revealed intramedullary lesion on T2- weighted-image at C2-C5 level. She was diagnosed as NMO with positive anti- AQP4 and probable SS. She received 1g methylprednisolone for 5 days proceeded with mycophenolic acid. One-year observation showed clinical improvement. Systemic autoantibodies must substantially be evaluated in NMO. Comprehensive diagnosis and providing appropriate immunosuppressant might prevent further disability and relapse.
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spelling doaj.art-72ebcc938a1245d4ab358cf12523f0f92023-02-02T03:12:29ZengMDPI AGNeurology International2035-83852035-83772019-03-0111110.4081/ni.2019.7958Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibodyRiwanti Estiasari0Salsabila Firdausia1Dewi Wulandari2Kartika Maharani3Freddy Sitorus4David Pangeran5Darma Imran6Department of Neurology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaDepartment of Neurology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaDepartment of Clinical Pathology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaDepartment of Neurology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaDepartment of Neurology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaDepartment of Neurology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaDepartment of Neurology, Faculty of Medicine, Universitas Indonesia, dr. Cipto Mangunkusumo General Hospital, JakartaNeuromyelitis Optic (NMO) is an inflammatory disorder involving central nervous system which often co-exists with other autoimmune diseases such as Sjögren’s syndrome (SS). NMO manifestation could precede or follow SS, but the role of anti-SSA in the pathogenesis of NMO remains unclear. We present a case of NMO with anti-AQP4 anti-SSA antibody positive. A-44-year-old female presented with right side weakness. The symptoms began with numbness that improved spontaneously. She also complained pain and dry sensations on her eyes. Schirmer test on her left eye, antinuclear antibody (ANA) and anti- SSA antibody were positive. Cervical MRI revealed intramedullary lesion on T2- weighted-image at C2-C5 level. She was diagnosed as NMO with positive anti- AQP4 and probable SS. She received 1g methylprednisolone for 5 days proceeded with mycophenolic acid. One-year observation showed clinical improvement. Systemic autoantibodies must substantially be evaluated in NMO. Comprehensive diagnosis and providing appropriate immunosuppressant might prevent further disability and relapse.https://pagepress.org/journals/index.php/ni/article/view/7958NeuromyelitisOpticSjogrenAQP4Anti-SSA
spellingShingle Riwanti Estiasari
Salsabila Firdausia
Dewi Wulandari
Kartika Maharani
Freddy Sitorus
David Pangeran
Darma Imran
Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody
Neurology International
Neuromyelitis
Optic
Sjogren
AQP4
Anti-SSA
title Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody
title_full Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody
title_fullStr Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody
title_full_unstemmed Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody
title_short Neuromyelitis optic with positive Anti-AQP4 and Anti-SSA/Ro antibody
title_sort neuromyelitis optic with positive anti aqp4 and anti ssa ro antibody
topic Neuromyelitis
Optic
Sjogren
AQP4
Anti-SSA
url https://pagepress.org/journals/index.php/ni/article/view/7958
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