Results 11 to 20 of about 6,572 (224)
Rosai-Dorfman Disease in a 4-Month-Old Female Presenting With Cervical Lymphadenopathy. [PDF]
ABSTRACT Rosai‐Dorfman disease is a rare histiocytic disorder that can mimic malignancies. This case highlights the importance of immunohistochemistry in distinguishing RDD from lymphoproliferative neoplasms, ensuring accurate diagnosis and management.
Khan A+5 more
europepmc +2 more sources
Neuropsychological Aspects of a Patient With Intracranial Rosai-Dorfman Disease: Case Report. [PDF]
ABSTRACT Intracranial Rosai‐Dorfman disease (RDD) is rarely reported in the literature. Up to the present date, there are no documented studies regarding the neuropsychological aspects of a patient with this diagnosis. This study fills this gap, reporting a case of a patient with petroclival RDD, emphasizing the importance of cognitive investigation.
Veras C+6 more
europepmc +2 more sources
Temporal bone manifestation of primary extranodal Rosai–Dorfman disease: a case report
Background Rosai–Dorfman disease is a rare benign histiocytic disorder characterized in most cases by painless cervical adenopathy. Less than 10% of extranodal cases involve bony lesions. Primary bone Rosai–Dorfman disease in the absence of nodal disease
E. Koonar+3 more
doaj +1 more source
Intracranial Rosai-Dorfman Disease: pathophysiology, diagnosis and treatment [PDF]
Introduction and purpose: Rosai-Dorfman Disease (RDD), known also as sinus histiocytosis with massive lymphadenopathy(SHML) is a benign histiocytic proliferative syndrome. The etiology and pathogenesis of RDD remains unclear.
Dryla, Aleksandra+3 more
core +2 more sources
Rosai Dorfman Disease - A Rare Presentation of Cervical Lymphadenopathy - A Case Report [PDF]
Rosai Dorfman disease is an uncommon histiocytic disorder presenting as bilateral cervical lymphadenopathy in children and young adults. Under the revised classification of histiocytic disorders, it is classified in the` R’ group of histiocytosis ...
C. P. Luck+4 more
core +3 more sources
Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented.
Smily Sharma+3 more
doaj +1 more source
Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease [PDF]
: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. The disease mainly affects lymph node tissue, although it is rarely confined to the skin.
Ana Gameiro+3 more
doaj +1 more source
Rosai Dorfman disease is a rare histiocytic disorder of over-production of non-Langerhans histiocytes, which typically manifests with massive lymphadenopathy and sinonasal involvement.
Yi Li+5 more
doaj +1 more source
Context: Rosai–Dorfman disease, also known as Sinus histiocytosis with massive lymphadenopathy, is a benign proliferative disorder of histiocytes. It typically affects lymph nodes; however, extranodal disease is being increasingly reported.
Rallapalli Rajyalakshmi+5 more
doaj +1 more source
Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease
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 +1 more source