Results 1 to 10 of about 4,871,887 (153)

Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease [PDF]

Anais Brasileiros de Dermatologia, 2009
Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descrita pela primeira vez por Rosai e Dorfman em 1969. As manifestações clássicas incluem linfadenopatia cervical usualmente acompanhada por febre, leucocitose
Fábio Machado Landim, Helena de Oliveira Rios, Carolina Oliveira Costa, Roney Gonçalves Fechine Feitosa, Francisco Dário Rocha Filho, Adriana Alencar Araújo Costa   +5 more
doaj   +2 more sources

Temporal bone manifestation of primary extranodal Rosai–Dorfman disease: a case report

Journal of Medical Case Reports, 2023
Background Rosai–Dorfman disease is a rare benign histiocytic disorder characterized in most cases by painless cervical adenopathy. Less than 10% of extranodal cases involve bony lesions. Primary bone Rosai–Dorfman disease in the absence of nodal disease
E. Koonar, F. Ramazani, M. Hyrcza, J. Chau   +3 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, Changxing Liu, Jeffrey A. Koempel   +2 more
doaj   +2 more sources

Clinicopathological Features, Treatment Response, and Outcome of Rosai‐Dorfman Disease in Two Children [PDF]

Clinical Case Reports
Rosai‐Dorfman disease is a rare non‐Langerhans cell histiocytic disorder. It is common in male children and young adults of African descent. It is classified into sporadic and familial types.
George Evele, Kouya Francine, Richard Bardin   +2 more
doaj   +2 more sources

Multifocal Rosai Dorfman disease and simultaneous endometrioid ovarian cancer: a case report [PDF]

Journal of Medical Case Reports
Background Rosai Dorfman disease is a rare histiocytosis, which is characterized by accumulation of histiocytes in lymph nodes, but also in extranodal locations. Histologically, one of the key features of Rosai Dorfman disease is emperipolesis. Treatment
Nele Graf, Teresa Halbsguth, Sven Becker, Morva Tahmasbi Rad   +3 more
doaj   +2 more sources

Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report [PDF]

Anais Brasileiros de Dermatologia, 2010
A doença de Rosai-Dorfman, também denominada histiocitose sinusal com linfadenopatia maciça, é histiocitose de células não Langerhans, idiopática e de curso benigno.
Josie da Costa Eiras, Antônio Pedro Mendes Schettini, Livia Lima de Lima, Liana Hortência Miranda Tubilla, Rosa Maria Libório de Oliveira   +4 more
doaj   +2 more sources

Rosai-Dorfman disease of the oral cavity

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, Mounir Omami, Marwa Garma, Ahlem Bellalah, Sameh Sioud, Jamil Selmi   +5 more
doaj   +2 more sources

Spinal Rosai–Dorfman disease: Case report of a rare disorde [PDF]

The Egyptian Journal of Radiology and Nuclear Medicine, 2015
Background: Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy (SHML)) is a rare, histiocytic, lymphoproliferative disease of unknown etiology affecting young people with male predominance.
A. Elsotouhy, M. Abozed, A. Marioud, A. Haider, A. Roux   +4 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, Hadice Akyol, Oner Sakallioglu, Cahit Polat, Erol Keles, Ozkan Alatas   +5 more
doaj   +2 more sources

Review and a case of rare Rosai-Dorfman disease

Biotechnology & Biotechnological Equipment
Rosai-Dorfman (RDD) is a rare histiocytic syndrome with variable clinical characteristics and extranodal involvement in more than 43% of the patients. This mini-review presents an overview of the literature on Rosai-Dorfman disease.
Dragomira Nikolova, Aleksandar Yordanov, Aleksandra Maslarova, Radka Hristoskova, Vera Damyanova, Savina Hadjidekova, Atanas Radinov   +6 more
doaj   +2 more sources