Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]
Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology typically characterized by cervical lymphadenopathy. Extranodal involvement often manifests in the head and neck region. We present a 10-year-old male who presented to
Kevin Hur +2 more
doaj +8 more sources
Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis [PDF]
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 +4 more sources
Rosai-Dorfman disease of the oral cavity [PDF]
First described by J Rosai and R F Dorfman in 1969, Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology. It is usually seen in the first two decades of life.
Abir Charfeddine +5 more
doaj +3 more sources
Radiology-pathology correlation: Rosai-Dorfman disease. [PDF]
Rosai–Dorfman Disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytic neoplasm. Although the disease classically presents as massive painless lymphadenopathy in young adults, RDD can also ...
Benson JC +7 more
europepmc +2 more sources
Intracranial Rosai-Dorfman Disease [PDF]
Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of ...
Yadav Arun Kumar +2 more
doaj +2 more sources
Rosai-Dorfman Disease Originating from Nasal Septal Mucosa [PDF]
Rosai-Dorfman disease is a rarely seen disease with unknown etiology. Extranodal involvement is most commonly seen in the head and neck region. Histopathologically, it is characterized by histiocytic cell proliferation. This paper presents a case of a 15-
Abdulvahap Akyigit +5 more
doaj +3 more sources
Anaesthesia for proximal femoral nailing in a patient with “Rosai Dorfman disease” with prior laryngotracheal reconstruction - Not all rosy as it seems [PDF]
Rosai Dorfman disease is a rare disease with massive lymphadenopathy. It presents significant challenges to the anaesthesiologists involving multiple organs especially the airway.
Ashna Shetty +4 more
doaj +2 more sources
Rosai-Dorfman disease mimicking gastrointestinal tuberculosis and fungal sinusitis: A case report
Every organ can be affected by Rosai-Dorfman disease, the most common being skin and soft tissue, bone and upper respiratory tract. Here we present a Rosai-Dorfman disease patient who manifested with multiple organ involvement.
Seid Getahun Abdela, MD +1 more
doaj +1 more source
Temporal bone manifestation of primary extranodal Rosai–Dorfman disease: a case report
Background Rosai–Dorfman disease is a rare benign histiocytic disorder characterized in most cases by painless cervical adenopathy. Less than 10% of extranodal cases involve bony lesions. Primary bone Rosai–Dorfman disease in the absence of nodal disease
E. Koonar +3 more
doaj +1 more source
Rosai–Dorfman Disease between Proliferation and Neoplasia
Simple Summary Rosai–Dorfman disease (RDD) was a benign histiocytic proliferative disorder rather than a neoplastic process. Emergent molecular studies have shown recurrent somatic gain-of-function mutations in genes of the MAPK pathway (e.g., NRAS, KRAS,
Ismail Elbaz Younes +2 more
semanticscholar +1 more source

