Results 81 to 90 of about 4,878 (159)

Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT This case highlights the possibility that Immunoglobulin G4‐related disease (IgG4‐RD) lesions can also occur in the sternoclavicular joint. If a neoplastic lesion is found in the sternoclavicular joint, a biopsy should be attempted to diagnose IgG4‐RD as a differential.
Remi Mizuta, Shinnosuke Takemoto, Mutsumi Ozasa, Sawana Ono, Takahito Fukuda, Ryuta Tagawa, Fumiko Hayashi, Kazumasa Akagi, Hiromi Tomono, Hirokazu Taniguchi, Midori Matsuo, Hiroshi Gyotoku, Takahiro Takazono, Hiroshi Ishimoto, Noriho Sakamoto, Keitaro Matsumoto, Yasushi Obase, Tomoya Nishino, Hiroshi Mukae   +18 more
wiley   +1 more source

A rare presentation of Rosai-Dorfman disease as a single dural-based lumbar intradural lesion: A case report

Heliyon
Central nervous system Rosai Dorfman disease (RDD) is a rare condition and it is just reported in 5% of 600 registered RDD cases. In previously reported patients, the intradural extramedullary spinal lesion is extremely rare.
Farid Kazemi Gazik, Peyman Gookizadeh, Masoud Khadivi, Ali Zare Mehrjardi, Arad Iranmehr   +4 more
doaj   +1 more source

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, Gudinchet, François, Hanquinet, Sylviane, Schmidt, Sabine, Tschäppeler, Heinz, Waibel, Peter   +5 more
core  

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

Anais 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, Adrilena Lopes Adriano, Marcelle Parente Breckenfeld, Igor Santos Costa, Antônio Renê Diógenes de Sousa, Heitor de Sá Gonçalves   +5 more
doaj  

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

, 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, Roballo, Carla Adriane, Sales, Guilherme Moura, Soares, Renata Fernandes Mendes   +3 more
core   +2 more sources

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, A. Greco, C. G. Cattaneo, M. de Vincentiis, M. Fusconi, M. Ralli   +5 more
core   +1 more source

A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease

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

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, K K Odinaka, Ukah Cornelius Ozobia   +2 more
doaj  

Langerhans´cell histiocytosis [PDF]

, 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

Rosi-Dorfman Syndrome; A case Report [PDF]

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, چینی فروش, میرمهدی   +1 more
core