Results 61 to 70 of about 11,417 (249)
Ophthalmic Rosai–Dorfman disease: a multi-centre comprehensive study
BMC Ophthalmology, 2021 Background To provide basic demographic information and clinicopathologic features of ophthalmic Rosai–Dorfman disease (RDD) with a literature review.
Tariq A Alzahem +4 more
semanticscholar +1 more source
Rosai-Dorfman Disease Presenting as Recurrent Nasal Polyposis
Philippine Journal of Otolaryngology Head and Neck Surgery, 2014 Objective: To present a case of Rosai-Dorfman disease in an individual with a 14-year history of recurrent nasal polyposis, and discuss its clinical presentation, physical examination, radiologic findings, histopathologic characteristics, and available ...
Neil Louis L. Apale +2 more
doaj +1 more source
Pediatric 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 with pulmonary involvement mimicking bronchogenic carcinoma
Journal 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
Bilateral breast Rosai‐Dorfman disease screen detected by mammography
Clinical 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
, 2018 Rosai-Dorfman disease is a rare, usually benign, entity that mostly affects children and adolescents. We report a clinical case in which the most common clinical and imaging manifestation is present: cervical lymphadenopathy. Histological confirmation is
Carvalho, André +5 more
core +2 more sources
BMC 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
Diagnosis of Rosai-Dorfman Disease by Fine Needle Aspiration Cytology in a Case with Cervical Lymphadenopathy and Nasal Mass [PDF]
, 2011 We report a case of Rosai-Dorfman Disease, a rare non neoplastic proliferative disorder of the cells of macrophage-histiocyte family, in a case with cervical lymphadenopathy and nasal mass diagnosed by fine needle aspiration ...
Jena, M
core +1 more source
Le syndrome de rosai dorfman de l’enfant (a propos d’un cas) [PDF]
, 2015 Le syndrome de rOSaï DOrFman ou histiocytose sinusale avec lymphadénopathie massive est une maladie rare d’étiologie inconnue, peut se voir à tout âge, l’enfant n’étant pas épargné.
Belaabida, B +4 more
core +2 more sources
Rosai-Dorfman Disease-Utility of 18F-FDG PET/CT for Initial Evaluation and Follow-up.
Clinical Nuclear Medicine, 2020 BACKGROUND The role of imaging in the management of Rosai-Dorfman disease (RDD), a rare non-Langerhans cell histiocytosis, is not clearly defined. We present an analysis of FDG PET/CT findings obtained for initial disease characterization, follow-up ...
S. Mahajan +8 more
semanticscholar +1 more source