Results 31 to 40 of about 11,417 (249)
Intracranial Rosai-Dorfman Disease: pathophysiology, diagnosis and treatment [PDF]
, 2022 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
Diagnosis and treatment of Rosai-Dorfman disease of the spine: a systematic literature review
Systematic Reviews, 2021 Purpose To review and summarize the clinical features, diagnosis, treatment strategies, and prognosis of spinal Rosai-Dorfman disease (RDD). Methods RDD is also termed as sinus histiocytosis with massive lymphadenopathy.
P. Hu +3 more
semanticscholar +1 more source
Human Genomics, 2021 Background Mutations in the SLC29A3 gene, which encodes the nucleoside transporter hENT3, have been implicated in syndromic forms of histiocytosis including H syndrome, pigmented hypertrichosis with insulin-dependent diabetes, Faisalabad histiocytosis ...
H. Chouk +8 more
semanticscholar +1 more source
Orbital involvement in Rosai-Dorfman disease [PDF]
, 2011 A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni +4 more
core +2 more sources
Rosai Dorfman Disease - A Rare Presentation of Cervical Lymphadenopathy - A Case Report [PDF]
, 2023 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
Clinicopathological features, treatment approaches, and outcomes in Rosai-Dorfman disease
Haematologica, 2019 Rosai-Dorfman disease is a rare subtype of non-Langerhans cell histiocytosis. With the last major report published in 1990, there is a paucity of contemporary data on this disease.
G. Goyal +13 more
semanticscholar +1 more source
Rosai-Dorfman Disease of Bone and Soft Tissue.
Archives of Pathology & Laboratory Medicine, 2021 CONTEXT.— Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown pathogenesis that may be diagnostically difficult in extranodal sites.
R. A. García, Edward F Dicarlo
semanticscholar +1 more source
Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease
Anais Brasileiros de Dermatologia, 2009 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
Fine-needle aspiration cytology of Rosai-Dorfman disease of bone [PDF]
, 2008 Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare, benign self-limiting condition of unknown etiology. Less than a quarter of cases have only extranodal involvement and a few cases of skeletal involvement of Rosai-Dorfman
Jing, Xin +2 more
core +1 more source
Rosai-Dorfman disease mimicking images of meningiomas: Two case reports and literature review
Surgical neurology international, 2021 Background: Rosai-Dorfman disease (RDD) is a rare non-Langerhans cell histiocytic proliferative disorder classically as a massive cervical lymphadenopathy.
R. Tatit +6 more
semanticscholar +1 more source