Evidence map›Paper›PMID 34211664›Full record

ArticleJournal of community hospital internal medicine perspectives2021

A case of neuromyelitis optica spectrum disorder with coexisting systemic lupus erythematosus.

Vikram Sangani, Mytri Pokal, Mamtha Balla, Ganesh Prasad Merugu, Sreedhar Adapa, Srikanth Naramala, Venu Madhav Konala

Open access · goldAbstract read
In one paragraph

Article in Journal of community hospital internal medicine perspectives, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 7 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

7 authors at 5 institutions in 1 country.

Vikram SanganiHospitalist, Department of Internal Medicine, Quantum HC, Navicent Health, Macon, Georgia.ORCID https://orcid.org/0000-0002-8460-9838
Mytri PokalHospitalist, Department of Internal Medicine, Quantum HC, Navicent Health, Macon, Georgia.ORCID https://orcid.org/0000-0002-5158-8663
Mamtha BallaDepartment of Internal Medicine, University of Toledo and Promedica Toledo Hospital, Toledo, Ohio, USA.ORCID https://orcid.org/0000-0001-9414-8599
Ganesh Prasad MeruguDivision Chief and Geriatric Fellowship Program Director, Division of Geriatric Medicine, Department of Family Medicine, University of Toledo, Toledo, Ohio, USA.ORCID https://orcid.org/0000-0002-8283-1267
Sreedhar AdapaDepartment of Internal Medicine, Division of Nephrology, Adventist Medical Center, Hanford, California, USA.ORCID https://orcid.org/0000-0001-5608-5654
Srikanth NaramalaDepartment of Internal Medicine, Division of Rheumatology, Adventist Medical Center, Hanford, California, USA.ORCID https://orcid.org/0000-0003-1238-856X
Venu Madhav KonalaDepartment of Internal Medicine, Division of Medical Oncology, Ashland Bellefonte Cancer Center, Ashland, Kentucky, USA.ORCID https://orcid.org/0000-0003-1953-8815
Adventist HealthCare · USNavicent Health · USAshland Bellefonte Cancer Center · USProMedica Toledo Hospital · USUniversity of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuromyelitis Optica or Devic disease is changed to Neuromyelitis Optica spectrum disorder to include more diverse neurological and autoimmune manifestations. This is a severe relapsing autoimmune demyelinating disorder commonly affecting the optic nerve and spinal cord. It has been reported as either the first manifestation of SLE or as a coexisting condition with other autoimmune disorders commonly included but not limited to SLE and SS. We discussed a case of a 49-year-old female patient who was initially presented with a left-sided weakness that rapidly progressed to quadriparesis and bladder dysfunction within a few days. She had positive autoimmune serology tests for SLE posing a diagnostic challenge as SLE is associated with neurological manifestations. Due to a lack of definitive diagnostic criteria for SLE, presence of AQP-4 antibodies in CSF, and evidence of longitudinal extensive transverse myelitis in MRI cervical spine, we conclude that she has Neuromyelitis Optica spectrum disorder with probable SLE. It is possible that she may develop more signs and symptoms of SLE with time and will need close follow up. Timely diagnosis and prompt treatment are vital to decrease morbidity and mortality, as done in our case. The patient was started on high-dose steroids with significant improvement in her symptoms. These patients may need early treatment with plasmapheresis and long-term follow-up with immunotherapy to prevent relapse. There are few case reports in the literature, and more information is needed to understand and better diagnose NMO with coexisting SLE.

Indexed as

AQP-4 antibodieslongitudinal extensive transverse myelitisNeuromyelitis opticaoptic neuritisSLE

Identifiers

PMID34211664
PMCPMC8221122
OpenAlexW3173471384

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.