Results 91 to 100 of about 4,871,906 (165)

Acute renal failure in a patient with Rosai-Dorfman disease.

open access: yes, 1999
Acute renal failure developed in a 57-year-old woman who had Rosai-Dorfman disease diagnosed 1 year previously on a cervical lymph node. Organ imaging showed diffuse masses infiltrating both kidneys.
Li, P. K.   +8 more
core  

Rosai-Dorfman disease presenting as multiple soft tissue masses

open access: yes, 2005
Rosai-Dorfman disease is a rare clinical disorder which may present in many forms. While classically a disease of lymph nodes, soft tissue involvement is fairly common.
Robinson, Philip G   +4 more
core   +1 more source

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Enfermedad de Rosai-Dorfman cutánea [PDF]

open access: yes, 2002
Se presenta el caso de un paciente de 23 años de edad, sexo masculino, con cuadro clínico de ocho meses de evolución de nódulos eritematovioláceos en cara y tórax, sin ningún síntoma sistémico.
Rueda Plata, Ricardo   +1 more
core  

Pediatric isolated intraparenchymal cerebellar Rosai-Dorfman disease

open access: yes, 2017
We illustrate the imaging findings of a case of isolated intraparenchymal cerebellar Rosai-Dorfman disease (RDD) in a child, which to our knowledge is the first reported case of such lesion in a child.
Janet M. Bruner   +2 more
core   +1 more source

ePoster

open access: yes
European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Two Cases of Cutaneous Rosai-Dorfman Disease

open access: yes, 2004
Rosai-Dorfman disease (RDD) of sinus histiocytosis with massive lymphadenopathy (SHML) is a benign, idiopathic histiocytic proliferative disorder affecting lymph nodes as well as extranodal sites.
정기양   +3 more
core  

Issue Information

open access: yes
Clinical Case Reports, Volume 14, Issue 4, April 2026.
wiley   +1 more source

Rosai-Dorfman Disease With Novel BRAF Fusion Involving the Central Nervous System

open access: yes
Rosai-Dorfman disease is an uncommon histiocytic neoplasm that is often self-limiting; however, rarely, it exhibits aggressive behavior and may undergo biological transformation to histiocytic sarcoma.
Cassidy, Daniel P   +2 more
core   +1 more source

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