Evidence map›Paper›PMID 41762414›Full record

ArticleCerebellum (London, England)2026

Pembrolizumab-Responsive Cerebellar PML in Untreated Sarcoidosis: A Case Report.

Ella Jack-Kee, Natasha Hoyle, Marios Hadjivassiliou

Abstract readCase Reports
In one paragraph

Article in Cerebellum (London, England), 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

3 authors.

Ella Jack-KeeMedical School, The University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0009-0008-6579-0900
Natasha HoyleSheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK.
Marios HadjivassiliouSheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK. m.hadjivassiliou@sheffield.ac.uk.ORCID http://orcid.org/0000-0003-2542-8954

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progressive multifocal leukoencephalopathy (PML) is a rare but devastating demyelinating disease usually seen in immunocompromised patients. We describe a 52-year-old man with pulmonary sarcoidosis, who presented with progressive ataxia, dysarthria, and unsteadiness of gait. He was not on immunosuppressive therapy at the onset of balance problems. Initial imaging showed increased signal in the cerebellar peduncles suggestive of cerebellar variant of multiple system atrophy (MSA-C). Cerebellar biopsy revealed PML. The patient’s condition deteriorated until pembrolizumab, a PD-1 checkpoint inhibitor, was commenced. He subsequently showed slow but sustained clinical improvement, supported by radiological (reduced enhancement) and spectroscopic evidence (increased N-Acetyl Aspartate to Creatine ratio), and he remains stable four years later. This case highlights the diagnostic challenge of PML in the absence of ongoing immunosuppression, and illustrates the potential role of pembrolizumab as a disease-modifying therapy. Early recognition and consideration of immunotherapy may be critical to improving outcomes in this otherwise often fatal condition.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalCerebellar DiseasesLeukoencephalopathy, Progressive MultifocalSarcoidosisHumansMaleMiddle AgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalpembrolizumabAtaxiaCase ReportCerebellar PedunclesPembrolizumabProgressive Multifocal LeukoencephalopathySarcoidosis

Identifiers

PMID41762414
PMCPMC12950049

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.