Results 51 to 60 of about 4,029 (188)

Rosai-Dorfman disease and superinfection due to Salmonella enterica and Mycobacterium avium complex in a patient living with HIV

open access: yesIDCases, 2020
Rosai-Dorfman disease (RDD) a rare, non-malignant disease of histiocytic proliferation usually presents as a painless lymphadenopathy. It has been associated with autoimmune diseases, viral infections, and malignancies.
Alejandro Olmedo-Reneaum   +3 more
doaj   +1 more source

Unilateral inguinal lymphadenopathy in a 6-year-old girl: An unusual presentation of Rosai-Dorfman disease

open access: yesPediatric Hematology Oncology Journal, 2019
Rosai Dorfman disease (RDD) commonly presents as bilateral cervical lymphadenopathy in children and young adults. We herein report a young girl with unilateral inguinal lymphadenopathy as a rare presentation of RDD. Keywords: Child, Rosai Dorfman disease,
Rakesh Kumar Pilania   +3 more
doaj   +1 more source

Rosai-Dorfman Disease (Sinus Histiocytosis with Massive Lymphadenopathy): A Case Report [PDF]

open access: yes, 2003
Rosai-Dorfman disease is a rare benign idiopatic histiocytic proliferative disorder. It is also known as sinus histiocytosis with massive lymphadenopathy.
Erkan Özüdoğru   +4 more
core  

Subconjunctival Masses Associated With Central Nervous System Rosai–Dorfman Disease [PDF]

open access: yes, 2011
To describe a case of subconjunctival masses with multiple intracranial masses diagnosed as Rosai-Dorfman disease by biopsy. Case report. A 25-year-old white man presented with bilateral subconjunctival masses, left optic nerve pallor, and posterior ...
Micheline McCarthy   +9 more
core   +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

Progress in diagnosis and treatment of osseous Rosai-Dorfman disease

open access: yesZhongguo aizheng zazhi, 2019
Sinus histiocytosis with massive lymphadenopathy, also known eponymously as Rosai-Dorfman disease, is a rare disease that is defined as a self-limiting proliferation of non-Langerhans histiocytes.
卫愉轩, 董 扬
doaj  

Rosai-Dorfman disease with pulmonary involvement mimicking bronchogenic carcinoma

open access: yesJournal of Cardiothoracic Surgery, 2020
Background Rosai-Dorfman disease is a histiocytic lesion that affects lung rarely. Case presentation We present a 52-year-old female diagnosed with right intrabronchial mass invading the bronchial wall and the extrabronchial tissues with lymphadenopathy.
Haneen Al-Maghrabi   +4 more
doaj   +1 more source

Novel treatment options for subglottic stenosis in Rosai-Dorfman disease: A case report and review of the literature

open access: yesOtolaryngology Case Reports, 2022
Rosai-Dorfman disease is a rare non-Langerhans cell histiocytosis which classically presents with cervical lymphadenopathy. Extranodal disease in the head and neck is uncommon.
Melissa M. Liu   +2 more
doaj   +1 more source

Advanced MRI in Rosai–Dorfman disease: Correlation with histopathology [PDF]

open access: yes, 2011
Rosai-Dorfman disease is an idiopathic benign lymphoproliferative disorder that can, on rare occasions, cause intracranial or intraspinal lesions with non-specific features on conventional imaging. For this reason, its diagnosis is based on the classical
R. Neelima   +11 more
core   +1 more source

Isolated cerebral Rosai–Dorfman disease presenting as a sole mass protruding into the fourth ventricle: A case report

open access: yesRadiology Case Reports, 2021
Rosai–Dorfman disease is a non–Langherans cell histiocytosis typically revealed by a lymphadenopathy. Central nervous system involvement is rare, exceptionally isolated, and usually consists of dural masses mimicking meningioma.
Guillaume Friconnet, MD   +7 more
doaj   +1 more source

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