Adult-onset Still’s disease with disseminated intravascular coagulation and hemophagocytic syndrome: a case report

BACKGROUND: Adult-onset Still’s disease is a rare inflammatory condition of unknown origin characterized by high spiking fever, arthralgia, arthritis, myalgia, salmon-colored evanescent rash, and hepatosplenomegaly. The diagnosis of adult-onset Still’s disease requires the exclusion of other possibl...

Descripción completa

Detalles Bibliográficos
Autores principales: Mimura, Tetsuhiko, Shimodaira, Masanori, Kibata, Minoru, Tsukadaira, Akihiro, Shirahata, Kumiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307634/
https://www.ncbi.nlm.nih.gov/pubmed/25532568
http://dx.doi.org/10.1186/1756-0500-7-940

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307634/
https://www.ncbi.nlm.nih.gov/pubmed/25532568
http://dx.doi.org/10.1186/1756-0500-7-940

Ejemplares similares