Case report: BRAF-inhibitor therapy in BRAF-mutated primary CNS tumours including one case of BRAF-mutated Rosai-Dorfman disease [PDF]
, 2022 Christopher Cronin +9 more
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A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease
iRADIOLOGY, Volume 3, Issue 5, Page 370-371, October 2025.
Lin Chen, Rui Zhou
wiley +1 more source
Rosai-Dorfman disease in a 12-year-old Nigerian male
South African Journal of Child Health, 2016 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
Rosai-Dorfman disease with spontaneous resolution: case report of a child
Revista Brasileira de Hematologia e Hemoterapia, 2011 Rosai-Dorfman disease is a self-limiting condition caused by histiocyte proliferation within the sinusoids of lymph nodes and in extranodal tissue. It is a rare disease, particularly in children, that progresses with extensive lymphadenopathy. This paper
Felipe Barbosa Lima +4 more
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Rosai - Dorfman disease: a rare entity diagnosed at autopsy
Autopsy and Case Reports, 2013 Rosai-Dorfman disease (RDD) or Sinus histiocytosis with massive lymphadenopathy is a rare and benign histiocytic proliferative disorder first described by Juan Rosai and Ronald Dorfman in 1969, whose etiology remains unknown.
João da Costa Veloso Neto +2 more
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ROSAI DORFMAN DISEASE WITH EXTENSIVE BONY INVOLVEMENT- A DIAGNOSTIC DILEMMA
, 2023 Maria Zahid Ahmed +7 more
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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
doaj
Cutaneous Rosai-Dorfman disease: A separate clinical entity
Journal of Dermatology and Dermatologic Surgery, 2017 Rosai-Dorfman disease is a benign, self-limited non-Langerhans cell histiocytosis of unknown etiology. Its most common clinical feature is extraordinary massive painless cervical lymphadenopathy.
Tiffany Hinojosa +6 more
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Reconstruction of a Patient With Rosai-Dorfman Disease Using Ramus Graft and Osseointegrated Implants: A Case Report [PDF]
, 2010 Umut Tekin, Hakan H. Tüz, Ömer Günhan
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Rosai–Dorfman disease as chronic bilateral granulomatous anterior uveitis: A case report
SAGE Open Medical Case ReportsRosai–Dorfman disease is a rare non-Langerhans cell histiocytosis disorder, also known as sinus histiocytosis, with massive lymphadenopathy. Rosai–Dorfman disease is classified into nodal and extranodal diseases.
Yaninsiri Ngathaweesuk +1 more
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