Results 111 to 120 of about 10,310,741 (229)

Rosai-Dorfman disease presenting with extensive cutaneous manifestation - Case report Doença de Rosai-Dorfman com manifestação cutânea extensa - Relato de caso

open access: yesAnais Brasileiros de Dermatologia, 2013
Rosai-Dorfman disease is a benign, self-limited, idiopathic proliferative histiocytic disorder. It was first described in 1969 by Rosai and Dorfman. In its typical form the disease is characterized by extensive cervical lymphadenopathy associated with ...
Paula Azevedo Borges Leal   +5 more
doaj  

Rosai-Dorfman syndrome associated with systemic erythematous lupus: case report [PDF]

open access: yes, 2019
Objetivo: Relatar um caso de associação de Síndrome de Rosai-Dorfman e Lúpus Eritematoso Sistêmico acompanhado no ambulatório de Clínica Médica de nosso Hospital Universitário.
Bastos, Stéphany Oliveira   +3 more
core   +2 more sources

Langerhans´cell histiocytosis [PDF]

open access: yes, 2014
La histiocitosis de células de Langerhans (HCL), anteriormente conocida como histiocitosis X, es una enfermedad poco frecuente caracterizada por la acumulación y proliferación de histiocitos, eosinófilos y células de Langerhans, con inclusión de gránulos
Casanovas, A., Elena, G., Rosso, Diego
core   +1 more source

A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease

open access: yes
iRADIOLOGY, Volume 3, Issue 5, Page 370-371, October 2025.
Lin Chen, Rui Zhou
wiley   +1 more source

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  

Solitary fibrous tumor [PDF]

open access: yes, 2018
Solitary fibrous tumor (SFT) is a rare tumor of mesenchymal origin that account for less than 2% of all soft tissue masses. Initially identified in the pleura, SFT has been identified in multiple anatomic locations and can arise anywhere in the body. The
Davanzo, Brian   +4 more
core   +1 more source

Rosi-Dorfman Syndrome; A case Report [PDF]

open access: yes
Rosai-Dorfman disease1,2 ( RDD or sinus histiocytosis with massive lymphadenopathy, SHML) is a rare, benign proliferative disorder of histiocytes, sometimes showing familiar incidence, it is etiology is uncertain.
جوانپور, حنانه   +1 more
core  

Intraosseous Rosai-Dorfman disease diagnosed by touch imprint cytology evaluation: A case series [PDF]

open access: yes, 2018
Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease (RDD) is a rare benign disorder that primarily affects the lymph nodes. Localized lymphadenopathy is the most common clinical manifestation of this disorder.
Alvarez Alegret   +29 more
core   +2 more sources

Cyclin D1 expression and novel mutational findings in Rosai‐Dorfman disease

open access: yesBritish Journal of Haematology, 2019
Rosai‐Dorfman disease (RDD) is an enigmatic histiocytic disorder classically diagnosed by a distinctive combination of pathological features: emperipolesis, or migration of intact haematological cells through the voluminous cytoplasm of lesional ...
E. Baraban   +6 more
semanticscholar   +1 more source

Rosai-Dorfman disease with spontaneous resolution: case report of a child

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2011
Rosai-Dorfman disease is a self-limiting condition caused by histiocyte proliferation within the sinusoids of lymph nodes and in extranodal tissue. It is a rare disease, particularly in children, that progresses with extensive lymphadenopathy. This paper
Felipe Barbosa Lima   +4 more
doaj   +1 more source

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