Evidence map›Paper›PMID 39592527›Full record

ReviewJournal of hematopathology2024

BRAF V600E mutation and high expression of PD-L1 in Rosai-Dorfman disease: case report and review of the literature.

Farnoush M Moen, Mariam M Youssef, Mihir Shukla, Mary Lynn Nierodzik, Marius E Mayerhoefer, Christopher Park

Abstract readCase ReportsReview
In one paragraph

Review in Journal of hematopathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Farnoush M MoenDepartment of Pathology, NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA. fmmoen@ucdavis.edu.ORCID http://orcid.org/0009-0002-8059-0516
Mariam M YoussefDepartment of Pathology, NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA.
Mihir ShuklaDepartment of Medicine, NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA.
Mary Lynn NierodzikDepartment of Medicine, NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA.
Marius E MayerhoeferDepartment of Radiology, NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA.
Christopher ParkDepartment of Pathology, NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BRAF V600E mutations are frequently found in histiocytic/dendritic cell neoplasms such as Erdheim-Chester disease (ECD) and Langerhans cell histiocytosis (LCH), but few reports have also described BRAF mutations in Rosai-Dorfman disease (RDD), and even these cases may predominantly represent mixed histiocytosis. BRAF mutations have been studied in histiocytic/dendritic cell neoplasms and described to be associated with increased risk of relapse and long-term consequences, but few studies have examined BRAF V600E mutation in RDD, which is recognized as a neoplasm given the high frequency of MAPK pathway alterations. Here, we report a case of BRAF V600E-mutated RDD in a patient who presented with generalized lymphadenopathy. During our evaluation of this patient, we also found expression of PD-L1 in neoplastic histiocytes. During our review period, only few cases of RDD reported to harbor BRAF mutation or were evaluated for the expression of PDL1 by neoplastic cells. Given the potential challenges in distinguishing RDD from other histiocytic/dendritic cell neoplasms, including mixed histiocytosis with similar clinicopathological manifestations, we will discuss the current state of knowledge regarding the frequency and clinical impact of BRAF V600E in RDD, as well as the role of BRAF mutations in RDD pathogenesis. Distinction of BRAF V600E mutated histiocytic/dendritic cell neoplasms requires consideration of distinctive histopathological and immunophenotypic findings in appropriate clinical and radiologic setting. Given the increasing use of BRAF inhibitors as well as checkpoint blockade inhibitors to treat a number of cancers, we will discuss the clinical implications of the presence of BRAF V600E mutation and PD-L1 expression in RDD.

Indexed as

B7-H1 AntigenHistiocytosis, SinusProto-Oncogene Proteins B-rafAdultAmino Acid SubstitutionFemaleHumansMaleMiddle AgedMutationMutation, MissenseB7-H1 AntigenBRAF protein, humanCD274 protein, humanProto-Oncogene Proteins B-rafBRAF inhibitorsBRAF V600E mutationCheckpoint blockade inhibitorsErdheim-Chester diseaseHistiocytic/dendritic cell neoplasmsHistiocytosisMAPK pathwayPDL1 inhibitorsRosai-Dorfman disease

Identifiers

PMID39592527
PMCPMC11635026

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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.