Results 81 to 90 of about 7,279 (231)
Neurology and the histiocytoses: a case of Rosai-Dorfman-Destombes disease [PDF]
, 2022 The histiocytoses are a group of rare disorders characterised by the accumulation of neoplastic or non-neoplastic activated histiocytes in various tissues.
Blake, Julian +11 more
core
IgG4-related disease: A systematic review of this unrecognized disease in pediatrics [PDF]
, 2016 Background: Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibro-inflammatory condition with an unclear pathophysiological mechanism affecting different parts of the body.
Bramer, W.M. (Wichor) +6 more
core +4 more sources
Intracranial multifocal Rosai-Dorfman disease [PDF]
Neurology Neuroimmunology & Neuroinflammation, 2016 Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease (RDD), is an uncommon benign histioproliferative disorder with systemic symptoms and lymphadenopathy. Mostly affecting lymph nodes, RDD typically presents as substantial painless bilateral cervical lymphadenopathy associated with fever, leukocytosis, anemia ...
Chen, Han, Zhou, Haiyan, Song, Zhi
openaire +2 more sources
Extranodal (cutaneous) Rosai Dorfman: a rare presentation [PDF]
, 2017 Rosai Dorfman disease is a rare histiocytic disorder of unknown etiology commonly involving the cervical lymph nodes first described in 1969, Extranodal involvement is very rare.
Ghodake, Nishant, Khadatkar, Ashwini
core +2 more sources
Clinical Endocrinology, Volume 103, Issue 4, Page 605-611, October 2025.ABSTRACT Objective This study investigated the prevalence, characteristics, and endocrine implications of thyroid incidentalomas detected during lymphoma staging using FDG‐PET/CT. Design Retrospective cohort study. Patients A total of 795 adult patients with lymphoma who underwent FDG‐PET/CT for staging at a tertiary oncology centre were included ...
Marcos Tadashi Kakitani Toyoshima +10 more
wiley +1 more source
Eye &ENT Research, Volume 2, Issue 3, Page 151-163, September 2025.Abstract IgG4‐related chronic rhinosinusitis (IgG4‐related CRS) is gaining recognition among various specialized physicians. As a systemic disease involving multiple organs, IgG4‐related CRS is still not widely recognized as an independent clinical entity. Given the complexity of diagnosing autoimmune‐related multisystem diseases, early recognition and
Lianqi Wan +3 more
wiley +1 more source
Foot & Ankle Orthopaedics, 2021 Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with
Jasmin Mansoori DPM +4 more
doaj +1 more source
An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
, 2016 Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F. +5 more
core +2 more sources
Characteristics of histiocytic neoplasms presenting as breast masses
British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Theodore Vougiouklakis +10 more
wiley +1 more source
Histopathology, Volume 87, Issue 2, Page 258-269, August 2025.Pathohistological analysis of FDCS revealed a morphological spectrum and led to the identification of the adhesion molecule L1CAM as a novel diagnostic immunomarker for FDCS. Sequencing identified NFKBIA as the most frequently altered gene, of note, exclusively in cases with a predominant epithelioid cytomorphology.
Selina Schelbert +12 more
wiley +1 more source