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Intracranial Rosai-Dorfman Disease [PDF]
Case Reports in Radiology, 2014 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 +7 more sources
Concomitant sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) and diffuse large B-cell lymphoma: a case report [PDF]
Journal of Medical Case Reports, 2008 Introduction Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman Disease, is a rare and benign source of lymphadenopathy first described in 1969, which mimics neoplastic processes.
Moore James C +2 more
doaj +3 more sources
Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]
Case Reports in Otolaryngology, 2017 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]
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 +4 more sources
Rosai-Dorfman disease of the oral cavity [PDF]
Autopsy and Case Reports, 2023 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
A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations
Journal of Cutaneous Immunology and Allergy, 2023 Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito +3 more
doaj +2 more sources
Rosai-Dorfman Disease Originating from Nasal Septal Mucosa [PDF]
Case Reports in Otolaryngology, 2015 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
Extra Nodal (Cutaneous) Rosai Dorfman Disease
Online Journal of Health & Allied Sciences, 2020 Rosai-Dorfman disease is an extremely rare disorder characterized by proliferation and accumulation of histiocytes in lymph nodes, usually in the cervical region. In approximately 43% cases, this accumulation occurs in extra nodal sites such as the skin,
Talha Ahmed +5 more
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Isolated intramedullary Rosai-Dorfman disease
Surgical Neurology International, 2016 Kaichuang Yang +3 more
openalex +4 more sources
Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]
, 2018 The described clinical case presents 39-year-old patient with no clinically significant accompanying diseases. Since the beginning of October 2015, the patient has complained of fever, abdominal pain and generalized enlarged lymph nodes.
Gercheva, Liana +3 more
core +4 more sources