Document Detail

Hemophagocytic syndrome in adult-onset Still's disease (AOSD): A must for biologics?-Case report and brief review of the literature.
MedLine Citation:
PMID:  20383508     Owner:  NLM     Status:  In-Data-Review    
A case of adult-onset Still's disease complicated by hemophagocytic lymphohistiocytosis is reported. Its management is being discussed on the background of the latest literature with special regard on the use of high-dose corticosteroids and immunosuppressive agents.
Urs Bürgi; Adriana Mendez; Paul Hasler; Hans Dieter Hüllstrung
Related Documents :
20383508 - Hemophagocytic syndrome in adult-onset still's disease (aosd): a must for biologics?-ca...
991098 - The rare problem of late recurrence in neuroblastoma.
12000698 - Mesenteric panniculitis associated with abdominal tuberculous lymphadenitis: a case rep...
20166368 - Kienb?ck's disease in a 6-year-old boy.
20015078 - From meiosis to postmeiotic events: the secrets of histone disappearance.
24887578 - Malignant renal epithelioid angiomyolipoma with liver metastasis after resection: a cas...
Publication Detail:
Type:  Journal Article     Date:  2010-04-10
Journal Detail:
Title:  Rheumatology international     Volume:  32     ISSN:  1437-160X     ISO Abbreviation:  Rheumatol. Int.     Publication Date:  2012 Oct 
Date Detail:
Created Date:  2012-09-25     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8206885     Medline TA:  Rheumatol Int     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  3269-72     Citation Subset:  IM    
Department of Medicine, Kantonsspital Aarau, Aarau, Switzerland.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Characterization of virulence factors and genetic background of Staphylococcus aureus isolated from ...
Next Document:  Whole-body MRI in the childhood form of hypophosphatasia.