Complications of surgical treatment of Rosai–Dorfman disease: A case report and review

BACKGROUND: Rosai–Dorfman disease (RDD) was first described in 1969 as an idiopathic histiocytic proliferative disorder. It commonly presents as a massive and painless adenopathy. Until 1990, extranodal involvement of the central nervous system (CNS) was rare and reported in less than 5% of the tota...

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Detalles Bibliográficos
Autores principales: Tomio, Ryosuke, Katayama, Makoto, Takenaka, Nobuo, Imanishi, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279960/
https://www.ncbi.nlm.nih.gov/pubmed/22347671
http://dx.doi.org/10.4103/2152-7806.92161

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279960/
https://www.ncbi.nlm.nih.gov/pubmed/22347671
http://dx.doi.org/10.4103/2152-7806.92161

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