Results 91 to 100 of about 9,189,306 (207)

Common progenitor origin for Rosai–Dorfman disease and clear cell sarcoma

The Journal of Pathology, Volume 264, Issue 3, Page 243-249, November 2024.
Abstract Histiocytic neoplasms (HNs) in adults have been reported to be associated with a high prevalence of coexisting haematological and solid malignancies. While a proportion of coexisting HNs and haematological malignancies share identical genetic alterations, the genetic association between HNs and solid malignancies has scarcely been reported. We
Aki Sato, Nozomi Yusa, Hiroyuki Takamori, Eigo Shimizu, Kazuaki Yokoyama, Satoshi Ichikawa, Hisayuki Yokoyama, Yuki Kasahara, Kodai Enda, Fumiyoshi Fujishima, Ryo Ichinohasama, Yasunori Ota, Seiya Imoto, Yasuhito Nannya   +13 more
wiley   +1 more source

Rosai-Dorfman disease presenting with extensive cutaneous manifestation - Case report Doença de Rosai-Dorfman com manifestação cutânea extensa - Relato de caso

Anais Brasileiros de Dermatologia, 2013
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, Adrilena Lopes Adriano, Marcelle Parente Breckenfeld, Igor Santos Costa, Antônio Renê Diógenes de Sousa, Heitor de Sá Gonçalves   +5 more
doaj  

A rare presentation of Rosai-Dorfman disease as a single dural-based lumbar intradural lesion: A case report

Heliyon
Central nervous system Rosai Dorfman disease (RDD) is a rare condition and it is just reported in 5% of 600 registered RDD cases. In previously reported patients, the intradural extramedullary spinal lesion is extremely rare.
Farid Kazemi Gazik, Peyman Gookizadeh, Masoud Khadivi, Ali Zare Mehrjardi, Arad Iranmehr   +4 more
doaj   +1 more source

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

Journal of Cytology, 2011
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, Asha Agarwal, Sanjay Kala   +2 more
doaj   +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, K K Odinaka, Ukah Cornelius Ozobia   +2 more
doaj  

Rosai-Dorfman Disease Originating from Nasal Septal Mucosa

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, Hadice Akyol, Oner Sakallioglu, Cahit Polat, Erol Keles, Ozkan Alatas   +5 more
doaj   +1 more source

Case report: BRAF-inhibitor therapy in BRAF-mutated primary CNS tumours including one case of BRAF-mutated Rosai-Dorfman disease [PDF]

, 2022
Christopher Cronin, Ronan Andrew McLaughlin, Louise Lane, Francesca M. Brett, Michael Jansen, Niamh Bermingham, Gerald Wyse, Liam Grogan, Patrick G. Morris, Séamus O’Reilly   +9 more
openalex   +1 more source

Cyclin D1 expression and novel mutational findings in Rosai‐Dorfman disease

British Journal of Haematology, 2019
Rosai‐Dorfman disease (RDD) is an enigmatic histiocytic disorder classically diagnosed by a distinctive combination of pathological features: emperipolesis, or migration of intact haematological cells through the voluminous cytoplasm of lesional ...
E. Baraban, S. Sadigh, J. Rosenbaum, John S. Van Arnam, A. Bogusz, Chelsea R Mehr, A. Bagg   +6 more
semanticscholar   +1 more source

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, Pedro Samuel de Valões Barcelos, Ana Paula Nunes Constâncio, Cleto Dantas Nogueira, Antônio Aldo Melo-Filho   +4 more
doaj   +1 more source

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
openalex   +1 more source