Results 51 to 60 of about 11,417 (249)

Rosai-Dorfman disease with spine involvement

Medicine, 2022
Rationale: Rosai-Dorfman disease (RDD) is a rare, benign, self-limiting disease, also known as sinus histiocytosis with giant lymphadenopathy. Skeletal involvement is rare, and this isolated bone lesion usually occurs in adults with no other symptoms. It
Haoran Jiang, Jipeng Song, Wan‐Lung Lin, M.-G. Yi, M. Yao, Li-Xiang Ding   +5 more
semanticscholar   +1 more source

Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report

Anais Brasileiros de Dermatologia, 2010
A doença de Rosai-Dorfman, também denominada histiocitose sinusal com linfadenopatia maciça, é histiocitose de células não Langerhans, idiopática e de curso benigno.
Josie da Costa Eiras, Antônio Pedro Mendes Schettini, Livia Lima de Lima, Liana Hortência Miranda Tubilla, Rosa Maria Libório de Oliveira   +4 more
doaj   +1 more source

A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]

, 2015
Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme, Farrell, MD, Christopher J, Kenyon, MD, PhD, Lawrence C, Krupa, BS, Kelly, Krupa, BS, Kristin, Madineni, MD, Ravichandra   +5 more
core   +2 more sources

Extranodal rosai dorfman disease: a case report of single soft tissue cystic lesion [PDF]

, 2020
Rosai-Dorfman disease (RDD) is an uncommon benign histiocytic disorder. It is found worldwide and slightly more common among in men (1.4:1), affecting individuals are with an average age of 20.6 years. Extranodal tissue involvement is documented in 25-43%
Agrawal, Ruchi, Baro, Bhanita, Saha, Anurag   +2 more
core   +2 more sources

A Report of Rosai–Dorfman Disease in an Adolescent

Case Reports in Pediatrics, 2022
Rosai–Dorfman disease (RDD) is a rare disease of unknown cause. It is a benign self-limiting condition characterized by the accumulation of activated histiocytes in the sinusoids of lymph nodes and/or extranodal tissues.
Emmanuella Amoako, K. Danso, R. S. Akuaku, Kofi Ulzen-Appiah   +3 more
semanticscholar   +1 more source

Isolated cerebral Rosai–Dorfman disease presenting as a sole mass protruding into the fourth ventricle: A case report

Radiology Case Reports, 2021
Rosai–Dorfman disease is a non–Langherans cell histiocytosis typically revealed by a lymphadenopathy. Central nervous system involvement is rare, exceptionally isolated, and usually consists of dural masses mimicking meningioma.
Guillaume Friconnet, MD, Mathilde Duchesne, MD, PhD, Marcel Gueye, MD, François Caire, MD, PhD, Charbel Mounayer, MD, PhD, Jean-François Emile, MD, PhD, François Labrousse, MD, PhD, Aymeric Rouchaud, MD, PhD   +7 more
doaj   +1 more source

Asymptomatic flow of Rosai-Dorfman disease [PDF]

, 2014
Introduction. Sinus histiocytosis with massive lymphadenopathy is a rare benign self-limiting disease of unknown etiology. The salivary gland involvement, indicating the extranodal character of the disease, often presents a diagnostic dilemma ...
Bjelaković Bojko, Kesić Ljiljana, Kostić Miloš, Mihailović Dragan, Mijovićć Žaklina, Petrović Dragan, Petrović Milica, Petrović Slađana, Stanković Ana, Vučković Ivica, Živković Nikola   +10 more
core   +1 more source

Rosai-Dorfman disease. A legacy of Professor Rosai that is still not exploited completely

Pathologica, 2021
Summary Rosai-Dorfman disease (RDD) is a rare form of non-Langerhans cell histiocytosis described by Rosai and Dorfman in 1969. It is a fascinating disease characterized by accumulation of large, pale histiocytes, frequently showing the emperipolesis ...
C. Doglioni
semanticscholar   +1 more source

Rosai-Dorfman disease and superinfection due to Salmonella enterica and Mycobacterium avium complex in a patient living with HIV

IDCases, 2020
Rosai-Dorfman disease (RDD) a rare, non-malignant disease of histiocytic proliferation usually presents as a painless lymphadenopathy. It has been associated with autoimmune diseases, viral infections, and malignancies.
Alejandro Olmedo-Reneaum, Aaron Molina-Jaimes, Eliezer Conde-Vazquez, Stefania Montero-Vazquez   +3 more
doaj   +1 more source

Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1. [PDF]

, 2015
The histiocytoses are rare tumors characterized by the primary accumulation and tissue infiltration of histiocytes and dendritic cells. Identification of the activating BRAFV600E mutation in Erdheim-Chester disease (ECD) and Langerhans cell histiocytosis
Arceci, Robert J, Bender, Ryan P, Bilalovic, Nurija, Gatalica, Zoran, Millis, Sherri Z, Palazzo, Juan P., Swensen, Jeffrey, Von Hoff, Daniel, Vranic, Semir   +8 more
core   +3 more sources