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Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report.
Chiang, Sharon; Pet, Douglas B; Talbott, Jason F; LaHue, Sara C; Douglas, Vanja C; Rosendale, Nicole.
Afiliação
  • Chiang S; Department of Neurology and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA. Sharon.Chiang@ucsf.edu.
  • Pet DB; Departments of Physiology and Psychiatry and the Kavli Institute for Fundamental Neuroscience, University of California, San Francisco, San Francisco, CA, USA. Sharon.Chiang@ucsf.edu.
  • Talbott JF; Department of Neurology and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.
  • LaHue SC; Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, USA.
  • Douglas VC; Department of Neurology and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.
  • Rosendale N; Buck Institute for Research On Aging, Novato, CA, USA.
BMC Neurol ; 23(1): 62, 2023 Feb 07.
Article em En | MEDLINE | ID: mdl-36750779
ABSTRACT

BACKGROUND:

Gadolinium enhancement of spinal nerve roots on magnetic resonance imaging (MRI) has rarely been reported in spinal dural arteriovenous fistula (SDAVF). Nerve root enhancement and cerebrospinal fluid (CSF) pleocytosis can be deceptive and lead to a misdiagnosis of myeloradiculitis. We report a patient who was initially diagnosed with neurosarcoid myeloradiculitis due to spinal nerve root enhancement, mildly inflammatory cerebrospinal fluid, and pulmonary granulomas, who ultimately was found to have an extensive symptomatic SDAVF. CASE PRESENTATION A 52-year-old woman presented with a longitudinally extensive spinal cord lesion with associated gadolinium enhancement of the cord and cauda equina nerve roots, and mild lymphocytic pleocytosis. Pulmonary lymph node biopsy revealed non-caseating granulomas and neurosarcoid myeloradiculitis was suspected. She had rapid and profound clinical deterioration after a single dose of steroids. Further work-up with spinal angiography revealed a thoracic SDAVF, which was surgically ligated leading to clinical improvement.

CONCLUSIONS:

This case highlights an unexpected presentation of SDAVF with nerve root enhancement and concurrent pulmonary non-caseating granulomas, leading to an initial misdiagnosis with neurosarcoidosis. Nerve root enhancement has only rarely been described in cases of SDAVF; however, as this case highlights, it is an important consideration in the differential diagnosis of non-inflammatory causes of longitudinally extensive myeloradiculopathy with nerve root enhancement. This point is highly salient due to the importance of avoiding misdiagnosis of SDAVF, as interventions such as steroids or epidural injections used to treat inflammatory or infiltrative mimics may worsen symptoms in SDAVF. We review the presentation, diagnosis, and management of SDAVF as well as a proposed diagnostic approach to differentiating SDAVF from inflammatory myeloradiculitis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Medula Espinal / Fístula Arteriovenosa / Malformações Vasculares do Sistema Nervoso Central Tipo de estudo: Etiology_studies Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Medula Espinal / Fístula Arteriovenosa / Malformações Vasculares do Sistema Nervoso Central Tipo de estudo: Etiology_studies Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article