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Case Study: Rosai-Dorfman Disease and Its Multifaceted Aspects [PDF]
Daniela Oliveira Werneck Rodrigues,1,2 Roberta Wolp Diniz,2 Leonardo Cunha Dentz,1 Monica de Albuquerque Costa,3 Roberto Heleno Lopes,2 Lucas Fernandes Suassuna,4 Jane Rocha Duarte Cintra,2 Christian Domenge2 1Department of Medicine, Centro Universitário
Daniela De Oliveira Werneck Rodrigues +1 more
exaly +1 more source
Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement [PDF]
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala +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 +2 more sources
Rosai-Dorfman disease in a 12-year-old Nigerian male [PDF]
Rosai-Dorfman disease is a rare disorder of systemic histioproliferation, first described in 1969 by Juan Rosai and Ronald Dorfman. It is characterised by massive lymphadenopathy, particularly of the head and neck region, and it is sometimes associated ...
Jacintha Chinyere Elo-Ilo +2 more
doaj +1 more source
We describe two cases of Rosai-Dorfman disease. One of them had commonly described cervical adenopathy and the second with the very rare bilateral orbital involvement. Both our cases required treatment with steroids because of the danger of pressure symptoms and disfigurement and multiple episodes of high fever in one of them.
Madhumita, Nandi +5 more
openaire +4 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
Background: Sinus histiocytosis with massive lymphadenopathy, also known as Rosai–Dorfman disease, is a rare proliferation of non-Langerhans histiocytes.
Sharon L Kipfer +2 more
doaj +1 more source
Rosai–Dorfman disease of the breast [PDF]
A 56-year-old female was recalled for assessment following screening mammography that demonstrated a new 9-mm indeterminate density in the left breast. Clinical breast examination was normal. Ultrasound confirmed a 9-mm predominantly well-defined hypoechoic breast mass. Core biopsy demonstrated large histiocytes with emperipolesis and positive staining
Parkin, C K E +3 more
openaire +4 more sources
Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease [PDF]
: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. The disease mainly affects lymph node tissue, although it is rarely confined to the skin.
Ana Gameiro +3 more
doaj +1 more source
Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented.
Smily Sharma +3 more
doaj +1 more source

