Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.asjsur.2023.07.046 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Rosai-Dorfman-Destombes disease in adolescence with hearing and vision loss involvement: A multidisciplinary approach.
Eur J Ophthalmol
November 2024
Ophthalmology division, São José do Rio Preto Medical School (FAMERP), São José do Rio Preto, Brazil.
To report a rare case of Rosai-Dorfman-Destombes (RDD) disease in a teenage girl exhibiting mild fever, night chills, vertigo, and progressive bilateral vision and hearing loss. Case report of a 15-year-old girl who underwent extensive ophthalmic multimodal imaging and a comprehensive workup evaluation. Multiple choroid lesion masses in both eyes associated with systemic multifocal lymphadenopathy, involvement of the paranasal sinuses, and unusual intracranial manifestations well-shown by magnetic resonance imaging (MRI) and whole-body PET-scan.
View Article and Find Full Text PDFRosai-Dorfman sphenoorbital histiocytosis with intraparenchymal invasion: Do we have to consider this skull base pathology as a malignant disease?
Surg Neurol Int
September 2024
Center for Cranial Base Surgery, Hospital Angeles Pedregal, Mexico City, Mexico.
Article Synopsis
- Rosai-Dorfman disease (RDD) is a rare histiocytosis often presenting with systemic symptoms, but this case highlights its unusual progression to the brain after skull base involvement.
- The presented case involves a 57-year-old male with severe headaches and a tumor mass affecting several areas, culminating in surgical intervention that revealed RDD.
- The study emphasizes the need for timely surgical treatment to prevent local and systemic disease progression, despite RDD typically being regarded as benign.
Multifocal Intracranial Rosai-Dorfman Disease Mimicking Immunoglobulin G4-Related Pachymeningitis.
Neurology
September 2024
From the Department of Neurology, Kanazawa University Graduate School of Medical Sciences, Japan.
Management of intracranial Rosai-Dorfman disease: An institutional experience.
J Clin Neurosci
September 2024
Department of Neurosurgery, NIMHANS, Bangalore, India.
Objective: Rosai-Dorfman disease (RDD) is a rare benign proliferative disorder of histiocytes. The study discusses the intracranial RDD approach, its management, and its outcome.
Methods: It is a retrospective study performed in a tertiary center, the National Institute of Mental Health and Neuroscience, Bangalore, from January 2010 to December 2022.
Surgical resection of pediatric craniocervical junction Rosai-Dorfman histiocytosis-a case report and literature review.
Childs Nerv Syst
November 2024
Department of Neurosurgery, Baylor Scott and White Health, Temple, TX, 76508, USA.
Rosai-Dorfman disease (RDD) with craniocervical junction involvement is a rare clinical entity. We present herein a case of a pediatric patient with craniocervical junction RDD which was surgically treated. A 10-year-old female with a history of B-cell acute lymphoblastic leukemia (B-ALL) in remission and RDD presented with frontal migraine headaches.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!