Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Recurrent central nervous system Rosai-Dorfman disease with KRAS mutation: a case report.

Diagnostic pathology - 13 Feb 2023

Wang Qingyang, Ren Hongxiang, Zheng Liyuan, Wang Juan, Zhong Dingrong

Abstract excerpt

BACKGROUND: Rosai-Dorfman disease (RDD) is a rare, non-Langerhans cell histiocytosis of unknown etiology. we report a very rare case of recurrent central nervous system RDD with KRAS gene mutation and review the literature to improve our understanding of this disease. CASE PRESENTATION: A 19-year-old male patient was admitted to our hospital for headache. Cranial magnetic resonance imaging revealed a mass of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Central Nervous System
Share to Diagnosis, Differential
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Proto-Oncogene Proteins p21(ras)

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 36782249
DOI: 10.1186/s13000-022-01276-7
PMCID: PMC9926849

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recurrent central nervous system Rosai-Dorfman disease with KRAS mutation: a case report.PMID 36782249Read ↗

Primary Rosai-Dorfman disease of the central nervous system: A clinical, histological, and molecular appraisal.Semantic proximity Read ↗

Mutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai-Dorfman disease.Semantic proximity Read ↗

BRAF mutation leading to central nervous system rosai-dorfman disease.Semantic proximity Read ↗

How I Diagnose Rosai-Dorfman Disease.Semantic proximity Read ↗

Rosai-Dorfman disease in the central nervous system with two isolated lesions originated from a single clone: a case report.Semantic proximity Read ↗

Mediastinal Rosai-Dorfman Disease with KRAS mutation case report and literature review.Semantic proximity Read ↗

Clinicopathological features, treatment approaches, and outcomes in Rosai-Dorfman disease.Semantic proximity Read ↗

Erdheim-Chester Disease with a Posterior Fossa Tumour Mimicking Neurosarcoidosis: A Case Report.Semantic proximity Read ↗

Testicular Rosai-Dorfman disease clonally related to CMML – case report and literature reviewSemantic proximity Read ↗

Pediatric Langerhans Cell Histiocytosis with BRAF Mutation Affecting Sacral Vertebra: A Case Report and Disease Review.Semantic proximity Read ↗

Erdheim–Chester Disease Mimicking Wilms Tumor in a Child: A Diagnostic ChallengeSemantic proximity Read ↗

[Cutaneous Rosai-Dorfman disease with lack of BRAF-V600, KRAS or NRAS mutations: A reactive or neoplastic disorder?]Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.