Evidence map›Paper›PMID 39650880›Full record

ArticleCureus2024

From Dizziness to Dysphagia: A Complex Presentation of Lateral Medullary Syndrome.

Isabella Canut, Bilal Farooqui, Joshua Hickman

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

3 authors.

Isabella CanutNeurology, Philadelphia College of Osteopathic Medicine, Suwanee, USA.
Bilal FarooquiNeurology, Philadelphia College of Osteopathic Medicine, Suwanee, USA.
Joshua HickmanInternal Medicine, AdventHealth New Smyrna Beach, New Smyrna Beach, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lateral medullary syndrome (LMS), also known as Wallenberg syndrome, is a rare neurological condition most commonly resulting from occlusion of the posterior inferior cerebellar artery (PICA). This syndrome is characterized by a constellation of symptoms including vertigo, ataxia, sensory deficits, and cranial nerve abnormalities, which arise due to infarction of the lateral medulla. We report the case of a 74-year-old female patient with a history of hypertension who presented to the emergency department with acute onset of vertigo and an unsteady gait. Following a diagnosis of LMS confirmed with imaging of the brain, the patient's hospital course was further complicated with the onset of atrial fibrillation and dysphagia, necessitating gastrostomy tube placement. Despite the challenges, early intervention and multidisciplinary care helped stabilize her condition.

Indexed as

dysphagialateral medullary syndromepathophysiologyprognosisstrokevertigowallenberg’s syndrome

Identifiers

PMID39650880
PMCPMC11622530

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.