Results 11 to 20 of about 4,871,906 (165)
Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease [PDF]
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
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Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]
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
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Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report [PDF]
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
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Rosai-Dorfman disease of the oral cavity
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
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Spinal Rosai–Dorfman disease: Case report of a rare disorde [PDF]
Background: Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy (SHML)) is a rare, histiocytic, lymphoproliferative disease of unknown etiology affecting young people with male predominance.
A. Elsotouhy +4 more
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Review and a case of rare Rosai-Dorfman disease
Rosai-Dorfman (RDD) is a rare histiocytic syndrome with variable clinical characteristics and extranodal involvement in more than 43% of the patients. This mini-review presents an overview of the literature on Rosai-Dorfman disease.
Dragomira Nikolova +6 more
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Intracranial Rosai-Dorfman Disease
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
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Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala +2 more
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Rosai-Dorfman Disease Originating from Nasal Septal Mucosa [PDF]
Rosai-Dorfman disease is a rarely seen disease with unknown etiology. Extranodal involvement is most commonly seen in the head and neck region. Histopathologically, it is characterized by histiocytic cell proliferation. This paper presents a case of a 15-
Abdulvahap Akyigit +5 more
doaj +2 more sources
Rosai-Dorfman disease in a 12-year-old Nigerian male
Rosai-Dorfman disease is a rare disorder of systemic histioproliferation, first described in 1969 by Juan Rosai and Ronald Dorfman. It is characterised by massive lymphadenopathy, particularly of the head and neck region, and it is sometimes associated ...
Jacintha Chinyere Elo-Ilo +2 more
doaj +1 more source

