Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement
Journal 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 +1 more source
An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
, 2016 Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F. +5 more
core +2 more sources
Cyclin D1 expression and novel mutational findings in Rosai‐Dorfman disease
British 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 in a 12-year-old Nigerian male
South 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
Social geography of rhinoscleroma and qualitatively and quantitatively abnormal cell-mediated immunity [PDF]
, 2018 Rhinoscleroma is a progressive chronic granulomatous disease of the upper respiratory tract that may extend to the tracheobronchial tract. It is common belief that the pathology is determined by Klebsiella Rhinoscleromatis.
A. Ciofalo +5 more
core +1 more source
A Case Report Diagnosed with Rosai-Dorfman Disease by Voice Change [PDF]
, 2014 Rosai-Dorfman disease is a rare disorder of unknown of etiology and is usually associated with benign proliferation of hematopoietic and fibrous tissue that often manifest in the head and neck region.
최홍식
core
Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]
, 2018 The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg +5 more
core
Intraosseous Rosai-Dorfman disease diagnosed by touch imprint cytology evaluation: A case series [PDF]
, 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
Rosai-Dorfman disease with spontaneous resolution: case report of a child
Revista 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
Rosai - Dorfman disease: a rare entity diagnosed at autopsy
Autopsy and Case Reports, 2013 Rosai-Dorfman disease (RDD) or Sinus histiocytosis with massive lymphadenopathy is a rare and benign histiocytic proliferative disorder first described by Juan Rosai and Ronald Dorfman in 1969, whose etiology remains unknown.
João da Costa Veloso Neto +2 more
doaj +1 more source