Results 81 to 90 of about 4,871,906 (165)

A rare case of Rosai-Dorfman disease mimicking a malignant lymphoproliferative process and IgG4-related disease

open access: yes
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic disorder that often mimics malignancies and immune-mediated conditions such as IgG4-related disease (IgG4-RD).
Julia Maria Sołek   +6 more
core   +1 more source

Letter to the Editor: “Rosai Dorfman: Rare Cause of Cervical Lymphadenopathy”

open access: yesEar, Nose & Throat Journal
We read with great interest the article by Kobayashi KE et al. published in 2023 entitled: “Presentation of external ear Rosai–Dorfman disease with laryngeal involvement” and wish to reconnoiter Rosai–Dorfman Disease’s (RDD) clinical entities and the ...
Muhammad Raziin Zainal Abidin MB BCh BAO   +2 more
doaj   +1 more source

Rosai–Dorfman disease as chronic bilateral granulomatous anterior uveitis: A case report

open access: yesSAGE Open Medical Case Reports
Rosai–Dorfman disease is a rare non-Langerhans cell histiocytosis disorder, also known as sinus histiocytosis, with massive lymphadenopathy. Rosai–Dorfman disease is classified into nodal and extranodal diseases.
Yaninsiri Ngathaweesuk   +1 more
doaj   +1 more source

Extra Nodal (Cutaneous) Rosai Dorfman Disease

open access: yesOnline Journal of Health & Allied Sciences, 2020
Rosai-Dorfman disease is an extremely rare disorder characterized by proliferation and accumulation of histiocytes in lymph nodes, usually in the cervical region. In approximately 43% cases, this accumulation occurs in extra nodal sites such as the skin,
Talha Ahmed   +5 more
doaj  

Cutaneous Rosai-Dorfman disease

open access: yes, 2007
Rosai-Dorfman disease (RDD) is a rare benign proliferative disorder of histiocytes in the lymph nodes with or without extranodal involvement. RDD limited to the skin without nodal involvement, known as cutaneous Rosai-Dorfman disease, is very rare.
ZAINAB BINTI AWANG NGAH
core  

Atypical presentation of extranodal Rosai-Dorfman disease.

open access: yes, 2009
We describe a 42-year-old woman with progressive dyspnea on exertion resulting from pulmonary artery compression by a mediastinal mass due to extranodal Rosai-Dorfman disease.
Bavaria, Joseph E, MD   +3 more
core   +1 more source

A Rare Case of Pseudo-Malignant Paranasal Extranodal Rosai–Dorfman Disease

open access: yesEar, Nose & Throat Journal
Rosai–Dorfman disease is a very rare disease characterized by histiocytic accumulation in the head and neck region and lymph node enlargement. We report a rare pseudo-malignant paranasal extranodal Rosai–Dorfman disease. A 69-year-old-man presented nasal
Koichi Tamura MD   +6 more
doaj   +1 more source

Anaesthesia for proximal femoral nailing in a patient with “Rosai Dorfman disease” with prior laryngotracheal reconstruction - Not all rosy as it seems

open access: yesTrauma Case Reports
Rosai Dorfman disease is a rare disease with massive lymphadenopathy. It presents significant challenges to the anaesthesiologists involving multiple organs especially the airway.
Ashna Shetty   +4 more
doaj   +1 more source

Pontine Rosai-Dorfman disease in a child

open access: yes, 2015
Rosai-Dorfman Disease (RDD) is a benign histiocytic disorder that commonly presents with massive lymphadenopathy. Central nervous system (CNS) involvement is only 5 %; isolated CNS involvement is much rarer.
Saglam, Arzu   +5 more
core   +1 more source

A rare presentation of extra nodal rosai-dorfman disease (case report) [PDF]

open access: yes, 2020
Rosai-Dorfman disease is considered to be one of the rare idiopathic disorders characterized by nonpainful lymphadenopathy. We reported a case of Rosai Dorfman disease that was presented with an isolated temporoparietal mass in an old Somalian patient ...
Kassem, Maysoun   +3 more
core  

Home - About - Disclaimer - Privacy