Results 41 to 50 of about 6,572 (224)

Unmasking Rosai-Dorfman disease in a woman with cervical lymphadenopathy: a histopathological insight [PDF]

open access: yes, 2023
Rosai-Dorfman disease (RDD) also called as sinus histiocytosis with massive lymphadenopathy is a rare benign proliferative self‐limiting disease of the macrophage‐histiocyte cell family.
Doshi, Anoushka A., Nelekar, Shruti B.
core   +2 more sources

Endocrine Implications of Thyroid Incidentalomas Detected During Lymphoma Staging With 18F‐Fluorodeoxyglucose Positron Emission Tomography

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Objective This study investigated the prevalence, characteristics, and endocrine implications of thyroid incidentalomas detected during lymphoma staging using FDG‐PET/CT. Design Retrospective cohort study. Patients A total of 795 adult patients with lymphoma who underwent FDG‐PET/CT for staging at a tertiary oncology centre were included ...
Marcos Tadashi Kakitani Toyoshima   +10 more
wiley   +1 more source

Scleritis and anterior uveitis may herald the development of an epibulbar tumor in patients with extranodal Rosai-Dorfman disease: a case report

open access: yesBMC Ophthalmology, 2019
Background Rosai-Dorfman disease is a rare non–Langerhans cell histiocytosis. Ocular involvement is even rarer, mostly involving the orbit and eyelids, although marginal corneal ulcers, uveitis, and epibulbar masses have also been reported, and is ...
Yu-Kuei Lee   +3 more
doaj   +1 more source

Extranodal (cutaneous) Rosai Dorfman: a rare presentation [PDF]

open access: yes, 2017
Rosai Dorfman disease is a rare histiocytic disorder of unknown etiology commonly involving the cervical lymph nodes first described in 1969, Extranodal involvement is very rare.
Ghodake, Nishant, Khadatkar, Ashwini
core   +2 more sources

Morphological, immunohistochemical and molecular analysis of follicular dendritic cell sarcomas: L1CAM as a new diagnostic marker

open access: yesHistopathology, EarlyView.
Pathohistological analysis of FDCS revealed a morphological spectrum and led to the identification of the adhesion molecule L1CAM as a novel diagnostic immunomarker for FDCS. Sequencing identified NFKBIA as the most frequently altered gene, of note, exclusively in cases with a predominant epithelioid cytomorphology.
Selina Schelbert   +12 more
wiley   +1 more source

Rosai-Dorfman disease of the paranasal sinuses and orbit [PDF]

open access: yes, 2011
Rosai-Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a benign indolent disorder, characterized by enlarged lymph nodes filled with histiocytes. Extranodal involvement is uncommon.
Aggarwal, Shyam   +3 more
core   +1 more source

Rosai Dorfman Disease in Mandible: A Rare Case Report [PDF]

open access: yes, 2023
Rosai Dorfman disease is generally defined as a massive bilateral painless cervical lymphadenopathy accompanied with both fever and leukocytosis with neutrophilia.
Hassan Mirmohammad Sadeghi   +2 more
core   +1 more source

Mass‐Forming Variants in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis: Diagnostic Complexities in Granulomatous Disease. A Case Report

open access: yesACR Open Rheumatology, Volume 7, Issue 4, April 2025.
A middle‐aged woman presented with a granulomatous breast lesion in 2018. By 2021, antibiotic‐resistant pneumonia led to the discovery of granulomatous inflammation in the lung and thyroid. Initially misdiagnosed as Erdheim–Chester disease (ECD), she was treated with interferon without success.
Benedetta Fazzi   +4 more
wiley   +1 more source

Spinal Rosai–Dorfman disease: Case report of a rare disorde

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2015
Background: Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy (SHML)) is a rare, histiocytic, lymphoproliferative disease of unknown etiology affecting young people with male predominance.
A. Elsotouhy   +4 more
doaj   +1 more source

Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT This case highlights the possibility that Immunoglobulin G4‐related disease (IgG4‐RD) lesions can also occur in the sternoclavicular joint. If a neoplastic lesion is found in the sternoclavicular joint, a biopsy should be attempted to diagnose IgG4‐RD as a differential.
Remi Mizuta   +18 more
wiley   +1 more source

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