Evidence map›Paper›PMID 35487693›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2022

Neurosarcoidosis of the Cauda Equina: Clinical Course, Radiographic and Electrodiagnostic Findings, Response to Treatment, and Outcomes.

Gabriela Alejandra Bou, Rocio Garcia-Santibanez, Alexander Jordan Castilho, Spencer Kristian Hutto

Open access · goldAbstract read
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Gabriela Alejandra BouFrom the Neurology Residency Program (G.A.B.), and Division of Neuromuscular Medicine (R.G.-S.), Department of Neurology, Division of Neuroradiology (A.J.C.), Department of Radiology, and Division of Hospital Neurology (S.K.H.), Department of Neurology, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-2792-0953
Rocio Garcia-SantibanezFrom the Neurology Residency Program (G.A.B.), and Division of Neuromuscular Medicine (R.G.-S.), Department of Neurology, Division of Neuroradiology (A.J.C.), Department of Radiology, and Division of Hospital Neurology (S.K.H.), Department of Neurology, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0003-4602-1766
Alexander Jordan CastilhoFrom the Neurology Residency Program (G.A.B.), and Division of Neuromuscular Medicine (R.G.-S.), Department of Neurology, Division of Neuroradiology (A.J.C.), Department of Radiology, and Division of Hospital Neurology (S.K.H.), Department of Neurology, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-8537-2000
Spencer Kristian HuttoFrom the Neurology Residency Program (G.A.B.), and Division of Neuromuscular Medicine (R.G.-S.), Department of Neurology, Division of Neuroradiology (A.J.C.), Department of Radiology, and Division of Hospital Neurology (S.K.H.), Department of Neurology, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-5644-9638
Emory University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesSarcoidosis is a multisystem granulomatous disease affecting the nervous system in 3%-5% of cases. It can affect almost any component of the nervous system. Involvement of the cauda equina is an understudied phenotype, and questions remain regarding its natural history and optimal approach to management. This study aims to study the long-term clinical evolution of neurosarcoidosis affecting the cauda equina, response to treatment, and clinical and radiographic outcomes.

methodsPatients with neurosarcoidosis treated at Emory University between January 1, 2011, and December 8, 2021, were retrospectively evaluated for manifestations of cauda equina disease and included if disease of the cauda equina could be substantiated by MRI or EMG.

resultsOf 216 cases, 14 (6.5%) involved the cauda equina. The median age was 49.5 years, and most were female (85.7%) and African American (64.3%). Chronic (>28 days) presentations were most common (78.6%), but acute (<7 days, 14.3%) and subacute (7-28 days, 7.1%) were also seen. The median modified Rankin Scale (mRS) score at nadir was 3 (range 2-4). Symptoms were asymmetric in 78.6% and included leg numbness (85.7%), leg weakness (64.3%), perineal numbness (35.7%), pain (42.3%), and incontinence (21.4%). On MRI, the cauda equina enhanced in 100%, appeared nodular in 78.6%, and was diffusely involved in 71.4%. Coexisting myelitis was common (cervical 28.6%, thoracic 35.7%, and conus medullaris 28.6%). Intracranial inflammation included leptomeningitis (71.4%) and cranial neuropathies (57.1%). Electrodiagnostic studies were conducted in 3 with only one showing features consistent with a radicular process. Serum and CSF angiotensin-converting enzyme levels were elevated in 38.5% and 0.0%, respectively. CSF white blood cell and protein were elevated in 92.9%. Corticosteroids were tried in all patients with durable stabilization or improvement in only 3 (21.4%). Second-line agents associated with improvement included methotrexate/infliximab (3/4, 75%), methotrexate (3/4, 75.0%), and azathioprine (1/1, 100%). During a median follow-up of 22.5 months, the final median mRS score was 3. Relapses occurred at a median of 6 months in 21.4%. In 9 patients with MRI follow-up, 6 improved (66.7%), 1 stabilized (11.1%), and 2 worsened (22.2%). DISCUSSION: Characteristic features of cauda equina involvement by neurosarcoidosis include chronically delayed presentations, nodular enhancement on MRI, poor response to corticosteroids, and substantial resultant neurologic disability.

Indexed as

Cauda EquinaSarcoidosisCentral Nervous System DiseasesFemaleHumansHypesthesiaMaleMethotrexateRetrospective StudiesMethotrexate

Identifiers

PMID35487693
PMCPMC9128042
OpenAlexW4225258137

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.