Results 191 to 200 of about 9,189,306 (207)

Facial cutaneous Rosai-Dorfman disease treated with pulsed dye laser: a case report and literature review. [PDF]

An Bras Dermatol
Wang QX, Luo SY, Zhou KY, Fang S.
europepmc   +1 more source

A rare case of nodular plaque variant of cutaneous-only Rosai-Dorfman disease: A case report. [PDF]

SAGE Open Med Case Rep
Seale E, Spurr A, Bose R.
europepmc   +1 more source

Rosai-Dorfman disease differentiated from a posterior mediastinal tumour: a case report. [PDF]

J Surg Case Rep
Hirai Y, Takahashi Y, Kaki T, Shima A, Kanai K, Iwamoto R, Hirai I.   +6 more
europepmc   +1 more source

A Case of Rosai-Dorfman Disease Successfully Treated by Corticotherapy. [PDF]

Case Rep Hematol
Diallo AB, Ndiaye M, Seck M, Keita M, Bousso ES, Touré SA, Faye BF, Diop S.   +7 more
europepmc   +1 more source

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How I Diagnose Rosai-Dorfman Disease.

American Journal of Clinical Pathology, 2023
OBJECTIVES Rosai-Dorfman disease (RDD) is one of 3 major types of histiocytosis, along with Erdheim-Chester disease and Langerhans cell histiocytosis.
A. Ravindran, K. Rech
semanticscholar   +1 more source

Rosai-Dorfman Disease Displays a Unique Monocyte-Macrophage Phenotype Characterized by Expression of OCT2

American Journal of Surgical Pathology, 2020
Rosai-Dorfman disease (RDD) is a rare histiocytosis with heterogenous clinical features. In this study, we characterized the histologic and phenotypic features in 33 RDD patients to better define the pathologic diagnosis.
A. Ravindran, G. Goyal, R. Go, K. Rech
semanticscholar   +1 more source

A pure Cutaneous Rosai-Dorfman disease: case report and a review of the literature

Caspian Journal of Internal Medicine, 2022
Background: Cutaneous Rosai-Dorfman disease (CRDD) is a rare variant of benign histiocytic proliferative disorder limited to the skin. The underlying etiology is still unclear, but it had been claimed that infections, immunodeficiencies, and autoimmune ...
F. Montazer, S. Farahani, Zoha Shaka, Z. Aryanian, A. Goodarzi   +4 more
semanticscholar   +1 more source

68Ga-FAPI and 18F-FDG PET/CT Images of a Patient With Rosai-Dorfman Disease With Liver Involvement.

Clinical Nuclear Medicine, 2022
Rosai-Dorfman disease is a rare non-Langerhans cell histiocytosis that is histopathologically characterized by the accumulation of CD68-positive and S100-positive histiocytes. The pathological changes are mostly discovered in lymph nodes.
Zhenying Chen, Qianqian Xue, Yun Yang, Hu Shun, Wei-bing Miao   +4 more
semanticscholar   +1 more source

BRAF mutation leading to central nervous system rosai‐dorfman disease

Annals of Neurology, 2018
Rosai–Dorfman disease (RDD) is an uncommon histiocytic proliferative disorder that can present in nodal, extranodal, or, extremely rarely, in central nervous system (CNS)‐restricted form.
T. Richardson, Megan B. Wachsmann, D. Oliver, Z. Abedin, Diana Ye, D. Burns, J. Raisanen, Benjamin M. Greenberg, K. Hatanpaa   +8 more
semanticscholar   +1 more source

Characterizing Rosai-Dorfman disease with [^18F]FDG PET/CT: a retrospective analysis of a single-center study

European Radiology, 2023
Jianan Zhang, R. Cui, Jian Li, Xin-xin Cao, Yaping Luo   +4 more
semanticscholar   +1 more source