Results 1 to 10 of about 1,910 (140)
Intracranial Rosai-Dorfman Disease [PDF]
Journal of Research in Medical Sciences, 2012 Rosai-Dorfman disease is a benign lymphohistiocytosis that often involve lymph nodes and present as massive lymphadenopathy with sinus histiocytosis. The disease is rarely associated with intracranial involvement.
Parvin Mahzoni +4 more
doaj +3 more sources
Temporal bone manifestation of primary extranodal Rosai–Dorfman disease: a case report [PDF]
Journal of Medical Case Reports, 2023 Background Rosai–Dorfman disease is a rare benign histiocytic disorder characterized in most cases by painless cervical adenopathy. Less than 10% of extranodal cases involve bony lesions. Primary bone Rosai–Dorfman disease in the absence of nodal disease
E. Koonar +3 more
doaj +4 more sources
Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease [PDF]
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 +3 more sources
Intracranial Rosai-Dorfman Disease [PDF]
Case Reports in Radiology, 2014 Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of other sites.
Yadav Arun Kumar +2 more
core +8 more sources
Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]
Case Reports in Otolaryngology, 2017 Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology typically characterized by cervical lymphadenopathy. Extranodal involvement often manifests in the head and neck region. We present a 10-year-old male who presented to
Kevin Hur +2 more
doaj +2 more sources
Rosai dorfman disease of the orbit [PDF]
Journal of Hematology & Oncology, 2008 To report the clinico-histopathologic features, management and outcome of Rosai-Dorfman disease of the orbit.Non-comparative case series.Rosai-Dorfman disease of the orbit constituted 0.09% of all ocular specimens received at our Institute, presenting with a firm rubbery mass causing proptosis; bilateral in 4 (57%) cases. The median age at presentation
Honavar Santosh G +2 more
openaire +5 more sources
Rosai-Dorfman disease of the oral cavity [PDF]
Autopsy and Case Reports, 2023 First described by J Rosai and R F Dorfman in 1969, Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology. It is usually seen in the first two decades of life.
Abir Charfeddine +5 more
doaj +2 more sources
Rosai-Dorfman disease of the lung [PDF]
Thorax, 2009 Rosai-Dorfman disease is a rare disorder which seems to involve not only the lymph nodes but most other organs of the body. The case history is presented of a woman who was thought to have atypical carcinoma of the lung but in whom a diagnosis of Rosai-Dorfman disease was eventually made following a range of investigations including CT scans, positron ...
A, Ali, D, Mackay
openaire +4 more sources
Systemic and Craniospinal Rosai Dorfman Disease with Intraparenchymal, Intramedullary and Leptomeningeal Disease [PDF]
International Journal of Hematology-Oncology and Stem Cell Research, 2021 Rosai Dorfman disease is a rare histiocytic disorder of over-production of non-Langerhans histiocytes, which typically manifests with massive lymphadenopathy and sinonasal involvement.
Yi Li +5 more
doaj +3 more sources
Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report [PDF]
Anais Brasileiros de Dermatologia, 2010 A doença de Rosai-Dorfman, também denominada histiocitose sinusal com linfadenopatia maciça, é histiocitose de células não Langerhans, idiopática e de curso benigno.
Josie da Costa Eiras +4 more
doaj +3 more sources