Evidence map›Paper›PMID 37773190›Full record

ReviewRevista medica del Instituto Mexicano del Seguro Social2023

[Weston-Hurst syndrome. A case report and literature review].

Arturo Eduardo Hernández-Lima, María Fernanda Pulido-Amaro, Carlos Yammir González-Rivera, Luis Guillermo Moreno-Madrigal, Diego Reyes-Vanegas

Open access · greenAbstract readReviewCase ReportsEnglish Abstract
In one paragraph

Review in Revista medica del Instituto Mexicano del Seguro Social, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 72% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 1 institution in 1 country.

Arturo Eduardo Hernández-LimaInstituto Mexicano del Seguro Social, Hospital General Regional No. 1 "Dr. Carlos Mac Gregor Sánchez Navarro", Departamento de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-1318-6102
María Fernanda Pulido-AmaroInstituto Mexicano del Seguro Social, Hospital General Regional No. 1 "Dr. Carlos Mac Gregor Sánchez Navarro", Departamento de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-9137-8521
Carlos Yammir González-RiveraInstituto Mexicano del Seguro Social, Hospital General Regional No. 1 "Dr. Carlos Mac Gregor Sánchez Navarro", Departamento de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-9298-8815
Luis Guillermo Moreno-MadrigalInstituto Mexicano del Seguro Social, Hospital General Regional No. 1 "Dr. Carlos Mac Gregor Sánchez Navarro", Departamento de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-8468-7318
Diego Reyes-VanegasInstituto Mexicano del Seguro Social, Hospital General Regional No. 1 "Dr. Carlos Mac Gregor Sánchez Navarro", Departamento de Medicina Interna. Ciudad de México, México.ORCID 0000-0002-9114-8144
Mexican Social Security Institute · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acute disseminated encephalomyelitis is an autoimmune and demyelinating disease. It is rare in adults. It has 3 main variants. One of them is Weston-Hurst syndrome, also called acute hemorrhagic leukoencephalitis. The objective was to share the experience in the diagnostic and therapeutic approach of this rare disease, as well as make a review of the current bibliography, in order to collaborate in the knowledge of this disease. Clinical case: 27-year-old woman, with a viral respiratory infection 2 weeks prior to the development of a neurological syndrome characterized by paresthesia, motor deficit, status epilepticus and acute encephalopathy, progressing rapidly to coma, with evidence in MRI of diffuse hemorrhagic lesions in cerebral white matter with demyelination and peripheral edema. It was administered steroid treatment for 5 days, with improvement of symptoms, but with motor and sensory deficits persisting. Conclusion: Acute disseminated encephalomyelitis and its variants are rare entities, with an important range of differential diagnosis, which must be identified and quickly treated to avoid their lethal or disabling outcome.

Indexed as

Encephalomyelitis, Acute DisseminatedLeukoencephalitis, Acute HemorrhagicStatus EpilepticusAdultFemaleHumansMagnetic Resonance ImagingAutoimmune DiseasesDemyelinating Autoimmune Diseases, CNSEncephalomyelitis, Acute DisseminatedLeukoencephalitis, Acute HemorrhagicMagnetic Resonance Imaging

Identifiers

PMID37773190
PMCPMC10599785
OpenAlexW4387075099

What OpenQuestion holds

Textmetadata
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.