Results 61 to 70 of about 283,013 (233)
Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature
Journal of the Belgian Society of Radiology, 2014 Rosai-Dorman disease (RDD) is a rare disorder of proliferative histiocytes with an unknown etiology. It is also known as sinus histiocytosis with massive lymphadenopathy. Most patients present with painless cervical lymphadenopathy due to accumulation of
H M Duijsens +4 more
doaj +1 more source
Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]
National Journal of Laboratory Medicine, 2018 Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan +4 more
doaj +1 more source
Rosacea in childhood and adolescence: A review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 6, Page 684-691, June 2025.Summary Despite presenting with similar symptoms, triggers, and progression patterns as adults, rosacea in children and adolescents is frequently overlooked as a primary differential diagnosis. However, initial manifestations of classic clinical types can be observed from infancy onwards.
Sören Korsing +4 more
wiley +1 more source
Rosai-Dorfman Disease: A Diagnostic Albatross in a Female Patient with Bilateral Persistent Neck Masses. A Case Report [PDF]
, 2012 RosaiDorfman disease (sinus histiocytosis with massive lymphadenopathy) is an uncommon benign and often self limiting lymphoproliferative disease of unknown aetiology which was first described by Rosai and Dorfman in 1969.
Akinbohun, AO +4 more
core +2 more sources
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 +18 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2014 Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limited, only involves skin and subcutaneous tissue and typically occurs as histiocyte-rich inflammatory infiltrates, manifesting as erythematous to brown ...
Han Ma +4 more
doaj +1 more source
International Archives of Otorhinolaryngology, 2014 Introduction Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement.
R. Pradhananga +3 more
semanticscholar +1 more source
Sinus Histiocytosis with Massive Lymphadenopathy ? Its Rare Immunological Complication
, 2015 A 3-year-old boy presented with irregular fever, multiple painless swelling over neck, axilla and inguinal region for one and half year. The child developed progressive pallor for one to two months.
Jagab, H. Ghosh, Joydeep Ghosh
semanticscholar +1 more source
Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]
, 2016 Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco +4 more
core
Concomitant sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) and diffuse large B-cell lymphoma: a case report [PDF]
, 2008 IntroductionSinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman Disease, is a rare and benign source of lymphadenopathy first described in 1969, which mimics neoplastic processes.
A Pulsoni +18 more
core +2 more sources