Results 11 to 20 of about 4,871,906 (169)

Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease [PDF]

open access: yesAnais 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   +2 more sources

Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]

open access: yesCase 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

Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report [PDF]

open access: yesAnais 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   +2 more sources

Rosai-Dorfman disease of the oral cavity

open access: yesAutopsy 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

Spinal Rosai–Dorfman disease: Case report of a rare disorde [PDF]

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2015
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
doaj   +2 more sources

Review and a case of rare Rosai-Dorfman disease

open access: yesBiotechnology & Biotechnological Equipment
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
doaj   +2 more sources

Intracranial Rosai-Dorfman Disease

open access: yesJournal 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   +1 more source

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

open access: yesJournal of Cytology, 2011
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
doaj   +2 more sources

Rosai-Dorfman Disease Originating from Nasal Septal Mucosa [PDF]

open access: yesCase Reports in Otolaryngology, 2015
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

open access: yesSouth African Journal of Child Health, 2016
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

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