Evidence map›Paper›PMID 41694903›Full record

ArticleCureus2026

Neurosarcoidosis: When Altered Mental Status Is a Sign of Systemic Disease.

Nidia Oliveira, Elisa Veigas, Tânia Batista, Luís Abreu, Marco Bousende

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. 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
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.

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.

Nidia OliveiraInternal Medicine, Unidade Local de Saúde de Viseu Dão-Lafões, Viseu, PRT.
Elisa VeigasInternal Medicine, Unidade Local de Saúde de Viseu Dão-Lafões, Viseu, PRT.
Tânia BatistaInternal Medicine, Unidade Local de Saúde de Viseu Dão-Lafões, Viseu, PRT.
Luís AbreuNeurology, Unidade Local de Saúde de Viseu Dão-Lafões, Viseu, PRT.
Marco BousendeNeuroradiology, Unidade Local de Saúde de Viseu Dão-Lafões, Viseu, PRT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoidosis is a systemic granulomatous disease of unknown etiology, characterized by a heterogeneous clinical course and the potential to affect any organ. Neurological involvement is rare and often mimics other nervous system disorders, with diagnosis based on the correlation of clinical, radiological, and histological findings, and biopsy of a suspected lesion serving as the definitive diagnostic method. We report the case of a 59-year-old woman, previously independent, who presented with progressive cognitive decline over 4-5 weeks, culminating in the inability to perform basic activities. Based on clinical, laboratory, and imaging findings, including magnetic resonance imaging and FDG-PET, a diagnosis of neurosarcoidosis (NS) was established, and oral corticosteroid therapy was initiated, resulting in significant clinical and imaging improvement. Although histological confirmation was not obtained, the integration of clinical and imaging findings provided consistent support for the diagnosis. This case highlights the importance of early recognition of NS, particularly in subacute presentations with cognitive impairment.

Indexed as

corticosteroid therapygranulomatous diseasesmultidisciplinary managementneurological manifestationsneurosarcoidosisrare clinical presentation

Identifiers

PMID41694903
PMCPMC12903030

What OpenQuestion holds

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Registered trials

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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.