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Clinical, histopathologic, and immunoarchitectural features of dermatopathic lymphadenopathy: an update
ArticleAbstract: Dermatopathic lymphadenopathy is a distinctive form of paracortical lymph node hyperplasia that usuaPalabras claves:Autores:Castellano-Sánchez A., Garces J.C., Khoury J.D., Li S., Medeiros L.J., Medina A.M., Miranda R.N., Patel K.P., Poppiti R.J., Sofía A. Garcés, Sriganeshan V., Thakral B., Xu J., Yin C.C.Fuentes:scopusFocal Rosai–Dorfman disease coexisting with lymphoma in the same anatomic site: a localized histiocytic proliferation associated with MAPK/ERK pathway activation
ArticleAbstract: Rosai–Dorfman disease is a rare histiocytic disorder shown to have gene mutations that activate thePalabras claves:Autores:González S., Johnson M.R., Khoury J.D., Li S., Manning J.T., Medeiros L.J., Molgó M., Patel K.P., Pina-Oviedo S., Ruiz-Cordero R., Sofía A. Garcés, Xu J., Yin C.C.Fuentes:scopusMutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai-Dorfman disease
ArticleAbstract: Rosai-Dorfman disease is a histiocytic disorder with a poorly defined pathogenesis. Recent molecularPalabras claves:Autores:Garces J.C., Khoury J.D., Li J., Li S., Medeiros L.J., Patel K.P., Pina-Oviedo S., Sofía A. Garcés, Yin C.C.Fuentes:scopus