Results 41 to 50 of about 10,310,741 (229)

Cerebral manifestation and diagnostic dilemma of Rosai-Dorfman disease

CNS Oncology, 2023
Rosai-Dorfman disease (RDD) is a rare, S100-positive histiocytic proliferation, that can cause both nodal and extranodal illness. We present a case of a 53-year-old male patient.
Szintia Almási, Tamás Pancsa, L. Tiszlavicz, A. Sejben   +3 more
semanticscholar   +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

Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene

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, Mohamed Ben Rejeb, L. Boussofara, Haїfa Elmabrouk, N. Ghariani, B. Sriha, A. Saâd, Dorra H’Mida, M. Denguezli   +8 more
semanticscholar   +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 rare entity: Case report in North Indian male

Asian Journal of Medical Sciences, 2014
Rosai Dorfman disease is a rare disease characterized by histiocytic proliferation of lymph node in young adults. We present here the case of a 67 years old Indian male presenting with lymphadenopathy and pyrexia of unknown origin for 16 months duration.
Ankur Baruah
doaj   +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, Paulo Eduardo Albuquerque Zito Raffa, Giovana Cassia de Almeida Motta, A. Bocchi, J. Guimaraes, P. Franceschini, P. H. D. de Aguiar   +6 more
semanticscholar   +1 more source

Rosai–Dorfman Disease: Breast Involvement—Case Report and Literature Review

Medicina, 2021
Background and objectives: Rosai–Dorfman disease (RDD) is a type of histiocytosis that usually appears in young adults or children as bilateral cervical lymphadenopathy, but extranodal involvement in not uncommon.
G. Iancu, N. Gică, L. Mustață, A. Panaitescu, D. Vasile, G. Peltecu   +5 more
semanticscholar   +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

Highlights of the Management of Adult Histiocytic Disorders: Langerhans Cell Histiocytosis, Erdheim-Chester Disease, Rosai-Dorfman Disease, and Hemophagocytic Lymphohistiocytosis

Clinical Lymphoma, Myeloma & Leukemia, 2020
Histiocytic disorders are an exceptionally rare group of diseases with diverse manifestations and a paucity of approved treatments, thereby leading to various challenges in their diagnosis and management. With the discovery of novel molecular targets and
Hind Salama, A. Jazieh, A. Alhejazi, A. Absi, S. Alshieban, M. Alzahrani, A. Alaskar, G. Gmati, M. Damlaj, K. Abuelgasim, A. Alghamdi, B. Alahmari, Areej Almugairi, Hazzaa AlZahrani, A. Bazarbachi, Mohamed O Musa, G. Goyal   +16 more
semanticscholar   +1 more source

Ophthalmic Rosai–Dorfman disease: a multi-centre comprehensive study

BMC Ophthalmology, 2021
Background To provide basic demographic information and clinicopathologic features of ophthalmic Rosai–Dorfman disease (RDD) with a literature review.
Tariq A Alzahem, A. Cruz, Azza M Y Maktabi, F. Chahud, H. Alkatan   +4 more
semanticscholar   +1 more source