Results 31 to 40 of about 10,310,741 (229)
Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease
Anais Brasileiros de Dermatologia, 2009 Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descrita pela primeira vez por Rosai e Dorfman em 1969. As manifestações clássicas incluem linfadenopatia cervical usualmente acompanhada por febre, leucocitose
Fábio Machado Landim +5 more
doaj +1 more source
Rosai Dorfman Disease - A Rare Presentation of Cervical Lymphadenopathy - A Case Report [PDF]
, 2023 Rosai Dorfman disease is an uncommon histiocytic disorder presenting as bilateral cervical lymphadenopathy in children and young adults. Under the revised classification of histiocytic disorders, it is classified in the` R’ group of histiocytosis ...
C. P. Luck +4 more
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Rosai-Dorfman Disease of Bone and Soft Tissue.
Archives of Pathology & Laboratory Medicine, 2021 CONTEXT.— Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown pathogenesis that may be diagnostically difficult in extranodal sites.
R. A. García, Edward F Dicarlo
semanticscholar +1 more source
Journal of Medical Case Reports, 2008 Introduction Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman Disease, is a rare and benign source of lymphadenopathy first described in 1969, which mimics neoplastic processes.
Moore James C +2 more
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Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment
Clinical Case Reports, 2021 Rosai‐Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai‐Dorfman disease, a case of 6‐year‐old boy with a history of multiple painless submandibular and cervical lymphadenopathy.
Kalpana Giri +3 more
doaj +1 more source
Potential role of 18F-FDG PET/CT in a case of progressive Rosai Dorfman disease [PDF]
Asia Oceania Journal of Nuclear Medicine and Biology, 2021 Rosai Dorfman disease is a rare form of nonlangerhans cell histiocytosis, presenting with extensive lymphadenopathies. Treatment in most cases of nodal disease, involves close observation; however, extranodal involvement requires a more definitive ...
Armaghan Fard-Esfahani +4 more
doaj +1 more source
Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature [PDF]
, 2016 Background: Rosai-Dorfman disease (RDD) is a rare form of histiocytosis characterized by histiocyte proliferation within lymph nodes and extranodal tissue. Here we report an unusual presentation of RDD in an Italian toddler.
Bruzzi, Patrizia +5 more
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Rosai-Dorfman disease presenting as stridor and hoarseness in a young female patient
Radiology Case Reports, 2023 Rosai-Dorfman disease is a non-Langherans cell histiocytosis typically revealed by lymphadenopathy. Extranodal involvement occurs in 43% and most commonly involves the head and neck, skin, and bones. Few reports have described laryngeal lesions.
Vivianne Kokje, MD, PhD +6 more
doaj +1 more source
Photodiagnosis and Photodynamic Therapy, 2023 Cutaneous Rosai-Dorfman Disease (CRDD), a rare form of Rosai-Dorfman Disease (RDD), lacks established treatment guidelines. In this case report, we detailed a successful case of CRDD management in a 50-year-old woman with facial lesions.
Runke Zhou +3 more
semanticscholar +1 more source
Fine-needle aspiration cytology of Rosai-Dorfman disease of bone [PDF]
, 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