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Non-demyelinating disorders mimicking and misdiagnosed as NMOSD: a literature review.
Zara, Pietro; Dinoto, Alessandro; Carta, Sara; Floris, Valentina; Turilli, Davide; Budhram, Adrian; Ferrari, Sergio; Milia, Stefania; Solla, Paolo; Mariotto, Sara; Flanagan, Eoin P; Lopez Chiriboga, A Sebastian; Sechi, Elia.
Afiliação
  • Zara P; Neurology Unit, Department of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
  • Dinoto A; Neurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Carta S; Neurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Floris V; Neurology Unit, Department of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
  • Turilli D; Neurology Unit, Department of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
  • Budhram A; Department of Clinical Neurological Sciences, Western University, London, Ontario, Canada.
  • Ferrari S; Neurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Milia S; Neurology Unit, Department of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
  • Solla P; Neurology Unit, Department of Medical, Surgical and Experimental Sciences, University of Sassari, Sassari, Italy.
  • Mariotto S; Neurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Flanagan EP; Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
  • Lopez Chiriboga AS; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Sechi E; Department of Neurology, Mayo Clinic, Jacksonville, Florida, USA.
Eur J Neurol ; 30(10): 3367-3376, 2023 10.
Article em En | MEDLINE | ID: mdl-37433584
ABSTRACT

BACKGROUND:

Differentiating neuromyelitis optica spectrum disorder (NMOSD) from its mimics is crucial to avoid misdiagnosis, especially in the absence of aquaporin-4-IgG. While multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein-IgG associated disease (MOGAD) represent major and well-defined differential diagnoses, non-demyelinating NMOSD mimics remain poorly characterized.

METHODS:

We conducted a systematic review on PubMed/MEDLINE to identify reports of patients with non-demyelinating disorders that mimicked or were misdiagnosed as NMOSD. Three novel cases seen at the authors' institutions were also included. The characteristics of NMOSD mimics were analyzed and red flags associated with misdiagnosis identified.

RESULTS:

A total of 68 patients were included; 35 (52%) were female. Median age at symptoms onset was 44 (range, 1-78) years. Fifty-six (82%) patients did not fulfil the 2015 NMOSD diagnostic criteria. The clinical syndromes misinterpreted for NMOSD were myelopathy (41%), myelopathy + optic neuropathy (41%), optic neuropathy (6%), or other (12%). Alternative etiologies included genetic/metabolic disorders, neoplasms, infections, vascular disorders, spondylosis, and other immune-mediated disorders. Common red flags associated with misdiagnosis were lack of cerebrospinal fluid (CSF) pleocytosis (57%), lack of response to immunotherapy (55%), progressive disease course (54%), and lack of magnetic resonance imaging gadolinium enhancement (31%). Aquaporin-4-IgG positivity was detected in five patients by enzyme-linked immunosorbent assay (n = 2), cell-based assay (n = 2 serum, 1; CSF, 1), and non-specified assay (n = 1).

CONCLUSIONS:

The spectrum of NMOSD mimics is broad. Misdiagnosis frequently results from incorrect application of diagnostic criteria, in patients with multiple identifiable red flags. False aquaporin-4-IgG positivity, generally from nonspecific testing assays, may rarely contribute to misdiagnosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Medula Espinal / Neuromielite Óptica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Medula Espinal / Neuromielite Óptica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália