Rosai-Dorfman disease is a benign, self-limited, idiopathic proliferative histiocytic disorder. It was first described in 1969 by Rosai and Dorfman. In its typical form the disease is characterized by extensive cervical lymphadenopathy associated with ...
Paula Azevedo Borges Leal +5 more
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Pitfalls and procedures in the histopathological diagnosis of oral and oropharyngeal squamous cell carcinoma and a review of the role of pathology in prognosis [PDF]
Triantafyllou, Asterios +1 more
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Intraoperative Frozen Section Diagnosis of Brain Rosai-Dorfman Disease Clinically and Radiologically Mimicking Meningioma. [PDF]
Hong J, Moes G, Lai J.
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Distinct Presentations of Langerhans Cell Histiocytosis in Children: A Case Series. [PDF]
Arega G +3 more
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Intracranial manifestations of adult Rosai-Dorfman disease: a systematic review and IPD meta-analysis of 327 cases. [PDF]
Perez-Chadid DA +11 more
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Introduction to the Review Series. Looking back and to the future: the Histiocyte Society blueprint for research in histiocytic disorders. [PDF]
Goyal G, Nanduri V.
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Rosai Dorfman Disease: A Myriad of Presentations-Multisystem Involvement Including Bone Marrow. [PDF]
Susai Manickam DJ +3 more
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Extranodal Rosai-Dorfman Disease in a Pediatric Patient: A Case Report. [PDF]
Miles L +4 more
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A Missed Case of Langerhans Cell Histiocytosis of the Proximal Femur after Total Hip Arthroplasty in an Adult: A Case Report. [PDF]
Sehrawat S +3 more
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Isolated osseous Rosai-Dorfman disease: a case report and review of literature. [PDF]
Sun JJ, Emert B, Dry S, Mofakham FA.
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