Cytophagic histiocytic panniculitis, hemophagocytic lymphohistiocytosis and undetermined autoimmune disorder: reconciling the puzzle

Cytophagic histiocytic panniculitis is a rare disease, associated with either nonmalignant conditions or subcutaneous panniculitis-like T-cell lymphoma, and often also associated with hemophagocytic lymphohistiocytosis (HLH). We report the case of a 11-year-old boy with a history of secondary HLH wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Pasqualini, Claudia, Jorini, Mauro, Carloni, Ines, Giangiacomi, Mirella, Cetica, Valentina, Aricò,, Maurizio, de Benedictis, Fernando Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974103/
https://www.ncbi.nlm.nih.gov/pubmed/24524345
http://dx.doi.org/10.1186/1824-7288-40-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974103/
https://www.ncbi.nlm.nih.gov/pubmed/24524345
http://dx.doi.org/10.1186/1824-7288-40-17

Ejemplares similares