Evidence map›Paper›PMID 41351624›Full record

SynthesisActa neurochirurgica2025

Intracranial manifestations of adult Rosai-Dorfman disease: a systematic review and IPD meta-analysis of 327 cases.

Daniela A Perez-Chadid, Aafreen Azmi, Jeremiah H Wijaya, Temitope Oshinowo, Juan P Avila-Madrigal, Aditi S Gorthy, Sri Sai Lakshman Akkineni, Andrew Egladyous, Nemanja Novakovic, Morana Vojnic and 2 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Acta neurochirurgica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Daniela A Perez-ChadidDepartment of Neurosurgery, New Jersey Medical School, Rutgers University, Newark, NJ, USA. Danielaperezchadid@gmail.com.
Aafreen AzmiDepartment of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.
Jeremiah H WijayaSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Temitope OshinowoDepartment of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.
Juan P Avila-MadrigalSchool of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
Aditi S GorthyDepartment of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.
Sri Sai Lakshman AkkineniDepartment of Medicine, Medical College of Georgia, Athens, GA, USA.
Andrew EgladyousDepartment of Neurosurgery, New Jersey Medical School, Rutgers University, Newark, NJ, USA.
Nemanja NovakovicDepartment of Neurosurgery, New Jersey Medical School, Rutgers University, Newark, NJ, USA.
Morana VojnicRutgers Cancer Institute, New Brunswick, NJ, USA.
Jonathan H ShermanDepartment of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.
Anil NandaDepartment of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rosai-Dorfman disease (RDD) is a rare non-Langerhans histiocytosis that involves the central nervous system (CNS) in approximately 5% of cases, most often presenting intracranially. While pediatric cases have been reported more frequently, adult intracranial RDD (IC-RDD) remains poorly characterized. We conducted a systematic review and individual patient data meta-analysis in accordance with PRISMA guidelines to define the epidemiology, clinical presentation, pathology, management strategies, and outcomes of adult IC-RDD. PubMed, Scopus, and the Cochrane Library were searched for histologically confirmed cases in adults over 18 years, and case reports, case series, and observational studies were included. Data were extracted on demographics, symptoms, imaging, histopathology, treatment, and outcomes. Primary endpoints were recovery and recurrence-free survival (RFS), with risk ratios (RRs) and 95% confidence intervals (CIs) calculated using random-effects models. A total of 327 patients from 186 studies met inclusion criteria. The median age was 43.6 years (range 18-83), with a male predominance (70.9%). The most common symptoms were headache (35.2%), seizures or loss of consciousness (28.7%), and visual disturbance (26.9%). Lesions were typically supratentorial intra-axial (52.9%) or extra-axial (20.5%). Surgical intervention was performed in 93.6% of patients, with gross total resection (GTR) achieved in 45.3%. At a median follow-up of 18.8 months, 37.9% achieved full recovery, 46.8% partial recovery, and 15.3% experienced recurrence, with a median RFS of 12 months. GTR was strongly associated with improved recovery (RR 0.26, 95% CI 0.19-0.37), whereas supratentorial intra-axial location (RR 0.56, 95% CI 0.41-0.75) and perilesional edema (RR 0.65, 95% CI 0.47-0.89) predicted poorer outcomes. These findings indicate that adult IC-RDD predominantly affects middle-aged men, presents with mass-effect symptoms, and has a location-dependent prognosis, with GTR conferring the best chance of recovery but recurrence remaining common and underscoring the need for long-term surveillance.

Indexed as

Histiocytosis, SinusAdolescentAdultFemaleHumansMaleMiddle AgedCentral nervous system histiocytosisGross total resectionIntracranial Rosai–Dorfman diseaseNeurologyNeurosurgeryNeurosurgical outcomes

Identifiers

PMID41351624
PMCPMC12682919

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.