Cargando…
AA amyloidosis in a patient with Langerhans cell histiocytosis
We report the case of a 37-year-old woman who presented with progressive renal dysfunction and proteinuria, in whom renal biopsy confirmed a diagnosis of AA amyloidosis. No evidence of chronic suppurative infection, connective tissue disease or malignancy was found. A past history of Langerhans cell...
Autores principales: | Thomson, Peter C., Taylor, Alison H.M., Morris, Scott T.W., Kipgen, David, Mactier, Robert A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421567/ https://www.ncbi.nlm.nih.gov/pubmed/25984125 http://dx.doi.org/10.1093/ndtplus/sfq201 |
Ejemplares similares
-
Langerhans cell histiocytosis
por: Kumar, Manish, et al.
Publicado: (2018) -
Langerhans Cell Histiocytosis of the Temporal Bone
por: Mayer, Scott, et al.
Publicado: (2020) -
Langerhans Cell Histiocytosis of the Tonsil
por: Cipolla, Federica, et al.
Publicado: (2022) -
Langerhans cell histiocytosis
por: Aruna, D. R., et al.
Publicado: (2011) -
Craniofacial and Intracranial Langerhans Cell Histiocytosis
por: Leenknegt, Benjamin, et al.
Publicado: (2020)