Neuromyelitis Optica (NMO) in Children: A Rare Case Report
Background: Neuromyelitis optica (NMO) is a rare autoimmune disease that covers 20-30% of diseases related to autoimmune disorders and about 1% of demyelination diseases. NMO symptoms are vary between individuals, there are generally 2 main symptoms, transverse myelitis and optic neuritis. This arti...
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Diponegoro University
2020
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oai:doaj.org-article:042a92cb85794b80849d03995a65c5f32021-11-05T16:47:43ZNeuromyelitis Optica (NMO) in Children: A Rare Case Report2503-217810.14710/jbtr.v6i3.8451https://doaj.org/article/042a92cb85794b80849d03995a65c5f32020-12-01T00:00:00Zhttps://ejournal2.undip.ac.id/index.php/jbtr/article/view/8451https://doaj.org/toc/2503-2178Background: Neuromyelitis optica (NMO) is a rare autoimmune disease that covers 20-30% of diseases related to autoimmune disorders and about 1% of demyelination diseases. NMO symptoms are vary between individuals, there are generally 2 main symptoms, transverse myelitis and optic neuritis. This article reported a child with NMO disease based on The Consensus of the International Panel for NMO Diagnosis (IPND) 2015. Case Presentation: An 8-year old boy with spastic tetraparesis, bilateral nervus opticus dysfunction, urinary retention, and allodynia et causa suspected NMO. Patient received therapy using high-dose intravenous methylprednisolone and showing a clinical improvement. Conclusion: This patient was diagnosed NMO based on IPND 2015 with an unknown AQP4-Ab status accompanied by supporting clinical symptoms. The management of NMO with high-dose intravenous methylprednisolone in this patient provides a meaningful response to the clinical improvement of the disease.Dodik TugasworoAditya KurniantoRetnaningsih RetnaningsihYovita AndhitaraRahmi ArdhiniTomy NugrohoJethro BudimanDiponegoro Universityarticleneuromyelitis opticaautoimmunemethylprednisoloneMedicine (General)R5-920ENJournal of Biomedicine and Translational Research, Vol 6, Iss 3, Pp 92-96 (2020) |
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neuromyelitis optica autoimmune methylprednisolone Medicine (General) R5-920 |
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neuromyelitis optica autoimmune methylprednisolone Medicine (General) R5-920 Dodik Tugasworo Aditya Kurnianto Retnaningsih Retnaningsih Yovita Andhitara Rahmi Ardhini Tomy Nugroho Jethro Budiman Neuromyelitis Optica (NMO) in Children: A Rare Case Report |
description |
Background: Neuromyelitis optica (NMO) is a rare autoimmune disease that covers 20-30% of diseases related to autoimmune disorders and about 1% of demyelination diseases. NMO symptoms are vary between individuals, there are generally 2 main symptoms, transverse myelitis and optic neuritis. This article reported a child with NMO disease based on The Consensus of the International Panel for NMO Diagnosis (IPND) 2015.
Case Presentation: An 8-year old boy with spastic tetraparesis, bilateral nervus opticus dysfunction, urinary retention, and allodynia et causa suspected NMO. Patient received therapy using high-dose intravenous methylprednisolone and showing a clinical improvement.
Conclusion: This patient was diagnosed NMO based on IPND 2015 with an unknown AQP4-Ab status accompanied by supporting clinical symptoms. The management of NMO with high-dose intravenous methylprednisolone in this patient provides a meaningful response to the clinical improvement of the disease. |
format |
article |
author |
Dodik Tugasworo Aditya Kurnianto Retnaningsih Retnaningsih Yovita Andhitara Rahmi Ardhini Tomy Nugroho Jethro Budiman |
author_facet |
Dodik Tugasworo Aditya Kurnianto Retnaningsih Retnaningsih Yovita Andhitara Rahmi Ardhini Tomy Nugroho Jethro Budiman |
author_sort |
Dodik Tugasworo |
title |
Neuromyelitis Optica (NMO) in Children: A Rare Case Report |
title_short |
Neuromyelitis Optica (NMO) in Children: A Rare Case Report |
title_full |
Neuromyelitis Optica (NMO) in Children: A Rare Case Report |
title_fullStr |
Neuromyelitis Optica (NMO) in Children: A Rare Case Report |
title_full_unstemmed |
Neuromyelitis Optica (NMO) in Children: A Rare Case Report |
title_sort |
neuromyelitis optica (nmo) in children: a rare case report |
publisher |
Diponegoro University |
publishDate |
2020 |
url |
https://doaj.org/article/042a92cb85794b80849d03995a65c5f3 |
work_keys_str_mv |
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