Results 61 to 70 of about 4,029 (188)

Extranodal Rosai-Dorfman disease with bilateral orbital involvement: Report of a case treated with systemic steroid alone [PDF]

open access: yes, 2008
Safiye Yilmaz1, Melih Ture1, Ahmet Maden1, Mine Tunakan21Department of Ophthalmology, 2Department of Pathology, Izmir Atatürk Training and Research Hospital, Izmir, TurkeyAbstract: We report the case of a 41-year-old female with bilateral ...
Safiye Yilmaz   +3 more
core  

Bilateral breast Rosai‐Dorfman disease screen detected by mammography

open access: yesClinical Case Reports, 2023
Rosai‐Dorfman disease (RDD) is a proliferative disorder of histiocytes typically found in nodal sites and commonly observed in females. Patients often present with systemic symptoms such as fever, lymphadenopathy, and weight loss.
Christina Sumner   +6 more
doaj   +1 more source

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

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

Rosai-Dorfman disease manifesting as a solitary mass with fat in the thymus a case report

open access: yesJournal of Cardiothoracic Surgery
Background Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a rare, self-limiting disease that predominantly affects children and young adults. Moreover, the disease is characterized by painless bilateral cervical
Dan Liu   +3 more
doaj   +1 more source

Isolated intraventricular Rosai–Dorfman disease

open access: yesAsian Journal of Neurosurgery, 2018
Rosai–Dorfman disease (RDD) is a benign histioproliferative disorder characterized by generalized lymphadenopathy, weakness, anemia, and rarely extranodal involvement. The disease affects the central nervous system (CNS) very rarely and at a relatively older age. Isolated intracranial involvement is very rare.
Patwardhan, Pranav Pramod   +1 more
openaire   +3 more sources

Fine-needle aspiration cytology of Rosai-Dorfman disease of bone [PDF]

open access: yes, 2008
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare, benign self-limiting condition of unknown etiology. Less than a quarter of cases have only extranodal involvement and a few cases of skeletal involvement of Rosai-Dorfman
Jing, Xin   +2 more
core   +1 more source

Diagnosis of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) by fine needle aspiration cytology

open access: yesJournal of Cytology, 2009
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.
Kushwaha Rashmi   +2 more
doaj  

Orbital Rosai–Dorfman disease: a case report and literature review

open access: yesJournal of International Medical Research, 2019
We report a case of orbital Rosai–Dorfman disease in a 45-year-old man who presented with exophthalmos as the first symptom for 6 months. He did not have any itching, photophobia, tears, headache, dizziness, nausea, vomiting, or other symptoms of ...
Xin Su, Liqing Zhang
doaj   +1 more source

Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]

open access: yesNational Journal of Laboratory Medicine, 2018
Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan   +4 more
doaj   +1 more source

Relapsing intracranial Rosai-Dorfman disease [PDF]

open access: yes, 2001
Two patients presenting with recurrent visual impairment due to relapsing intracranial Rosai-Dorfman disease are described. In both patients a preoperative diagnosis of meningioma was made. Histological examination disclosed the characteristic picture of
Thom, M   +3 more
core  

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