Evidence map›Paper›PMID 38303503›Full record

ArticleThe American journal of case reports2024

An AQP-4-IgG-Positive Patient with Neuroimaging Findings Suggestive of Multiple Sclerosis.

Mingxia Li, Shuangxi Liu, Jun Zhou, Liqian Xiao, Rongyong Man, Junjie Yin

Abstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mingxia LiDepartment of Neurology, Hunan University of Medicine General Hospital, Huaihua, Hunan, China (mainland).ORCID 0000-0002-7828-4985
Shuangxi LiuDepartment of Neurology, Hunan University of Medicine General Hospital, Huaihua, Hunan, China (mainland).
Jun ZhouDepartment of Neurology, Hunan University of Medicine General Hospital, Huaihua, Hunan, China (mainland).
Liqian XiaoDepartment of Health Management Center, Hunan University of Medicine General Hospital, Huaihua, Hunan, China (mainland).
Rongyong ManDepartment of Neurology, Hunan University of Medicine General Hospital, Huaihua, Hunan, China (mainland).
Junjie YinDepartment of Neurology, Hunan University of Medicine General Hospital, Huaihua, Hunan, China (mainland).ORCID 0000-0003-0400-1601

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Multiple sclerosis (MS) and neuromyelitis optica spectrum disorders (NMOSDs) are 2 similar but distinct diseases. These diseases were difficult to distinguish from each other until aquaporin-4-IgG (AQP-4-IgG) was discovered. The accurate identification of these 2 diseases is crucial for appropriate drug treatment in clinical practice. Herein, we report a case of AQP-4-IgG seroconversion with magnetic resonance imaging (MRI) findings suggestive of MS. CASE REPORT A 54-year-old woman developed weakness in her right lower extremity that gradually returned to normal 4 years ago. Recently, she was admitted to the hospital for numbness and weakness of both lower limbs and the right upper limb for more than 10 days. The clinical and MRI features of the patient suggested a high susceptibility for misdiagnosis of MS. However, careful observation of the MRI revealed the presence of atypical MS lesions ("red flag" signs), indicating the possibility of other diagnoses in this patient. After further examination, serum AQP-4-IgG was detected, suggesting the potential presence of another disorder, NMOSD, in the patient. CONCLUSIONS Attention should be given to the identification of MS MRI "red flag" signs. Even for patients with a high suspicion of MS, it is necessary to conduct antibody tests for AQP-4-IgG, MOG-IgG and other relevant markers to screen for associated diseases because MS disease-modifying therapy approaches may lead to a deterioration in the state of NMOSD patients. Analyzing this case can help us to further distinguish the differences between these 2 types of diseases, which has important practical clinical value.

Indexed as

Multiple SclerosisAquaporin 4AutoantibodiesFemaleHumansImmunoglobulin GMiddle AgedMyelin-Oligodendrocyte GlycoproteinNeuroimagingAquaporin 4AutoantibodiesImmunoglobulin GMyelin-Oligodendrocyte Glycoprotein

Identifiers

PMID38303503
PMCPMC10846751

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