Results 91 to 100 of about 11,417 (249)
A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations
Journal of Cutaneous Immunology and Allergy, 2023 Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito +3 more
doaj +1 more source
Emperipolesis in a Case of Adult T Cell Lymphoblastic Lymphoma (Mediastinal type)-Detected at FNAC and Imprint Cytology [PDF]
, 2011 Emperipolesis is a condition in which viable hematopoetic cells are seen intact in the cytoplasm of host cell without damage. This phenomenon is seen in many physiologic and pathologic conditions, its presence in Rosai Dorfman disease (RDD) is ...
Abhishekh, MG +3 more
core
Multimodality imaging manifestations of Rosai-Dorfman disease
Acta Radiologica Open, 2020 Background Rosai-Dorfman disease (RDD) is a rare lympho-histiocytic disorder of indeterminate etiology usually presenting with lymph node involvement, and infrequently with extra-nodal manifestations. The diagnosis of this condition is challenging due to
Tanvi Vaidya, A. Mahajan, S. Rane
semanticscholar +1 more source
ACR 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
Journal 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
Journal 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
Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report
Clinical 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
A Rare Case of Multiorgan Involvement of Rosai Dorfman Disease in an Elderly Female
Journal of Nepal Medical Association, 2014 Sinus histiocytosis with massive lymphadenopathy (SHML), Rosai-Dorfman Disease, is a rare histiocytic syndrome first described by Rosai and Dorfman, most frequently seen in children and young adults.The disease is more common in males and in individuals ...
Rakesh Digambar Waghmare
doaj +1 more source
Rosai-Dorfman syndrome associated with systemic erythematous lupus: case report [PDF]
, 2019 Objetivo: Relatar um caso de associação de Síndrome de Rosai-Dorfman e Lúpus Eritematoso Sistêmico acompanhado no ambulatório de Clínica Médica de nosso Hospital Universitário.
Bastos, Stéphany Oliveira +3 more
core +2 more sources
BRAF V600E mutation detected in a case of Rosai-Dorfman disease
Haematologica, 2018 Rosai-Dorfman Disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare, nonmalignant histiocytic proliferation of unknown etiology. According to the new classification, it belongs to the R group of histiocytoses.[1][1] The
G. Fatobene +8 more
semanticscholar +1 more source