Results 31 to 40 of about 4,871,906 (169)
Rosai-Dorfman Disease Isolated to the Thoracic Epidural Spine [PDF]
, 2015 Rosai-Dorfman disease is a rare benign histiocytic disease that infrequently presents in the spine. We report a case of Rosai-Dorfman disease isolated to the epidural thoracic spine in a 26-year-old male.
Bhavya Rehani +7 more
core +1 more source
Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
Case Reports in Medicine, 2016 Rosai-Dorfman disease is a rare, benign histiocytic proliferative disorder that usually affects the lymph nodes. Although extranodal involvement has been reported in diverse sites, manifestation in the cardiovascular system is extremely rare ...
Fandresena Arilala Sendrasoa +6 more
doaj +1 more source
Uveitic glaucoma and Rosai-Dorfman disease (sinus histiocytosis).
, 2006 PURPOSE: To report a novel association of uveitic glaucoma with Rosai-Dorfman disease. METHODS: Case report. RESULTS: A 67-year-old Caucasian woman presented with a chronic bilateral granulomatous uveitis which did not respond to conventional topical ...
Hundal, KS +8 more
core +1 more source
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 +3 more
doaj +1 more source
Rosai-Dorfman Disease Presenting as Recurrent Nasal Polyposis
Philippine Journal of Otolaryngology Head and Neck Surgery, 2014 Objective: To present a case of Rosai-Dorfman disease in an individual with a 14-year history of recurrent nasal polyposis, and discuss its clinical presentation, physical examination, radiologic findings, histopathologic characteristics, and available ...
Neil Louis L. Apale +2 more
doaj +1 more source
Cutaneous Rosai‐Dorfman Disease With MAP2K1 Mutation Treated With Encorafenib and Binimetinib
JEADV Clinical Practice, EarlyView.ABSTRACT Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unifocal to multisystemic involvement. Activating mutations in the MAPK/ERK pathway can occur in up to 50% of RDD cases. We report a case of cutaneous RDD (C‐RDD) with facial and truncal lesions harboring an activating MAP2K1 (MEK1) mutation that showed a complete response to a ...
Melike Ak +2 more
wiley +1 more source
Enfermedad de Rosai-Dorfman o histiocitosis sinusal con linfadenopatía masiva [PDF]
, 2019 Rosai-Dorfman Disease,or sinus histiocytosis with massive lymphadenopathy,is a chronic histiocytic spreading disorder with a benign process which in the majority of the cases has a tendency to spontaneous regression. The etiology is still unknown. It may
Primo, Lina +4 more
core
Pediatric Hematology Oncology Journal, 2019 Rosai Dorfman disease (RDD) commonly presents as bilateral cervical lymphadenopathy in children and young adults. We herein report a young girl with unilateral inguinal lymphadenopathy as a rare presentation of RDD. Keywords: Child, Rosai Dorfman disease,
Rakesh Kumar Pilania +3 more
doaj +1 more source
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Indeterminate cell histiocytosis (ICH) is a clonal proliferative disorder of mononuclear phagocyte cells that shows features of both dendritic and histiocytic cells. Only around 100 cases of ICH were reported, and among them, only 24% of reported cases involve pediatric patients, with a mean age at diagnosis of 50 years.
Seung‐Soo Lee +3 more
wiley +1 more source
Rosai-Dorfman Disease of the Breast [PDF]
, 2017 Rosai-Dorfman disease (also known as sinus histiocytosis with massive lymphadenopathy) is a rare benign proliferative disorder of histiocytes that typically involves the lymph nodes and can also involve extranodal sites. Rosai-Dorfman disease confined to
Larkin, Anne C. +4 more
core +1 more source