| Literature DB >> 24739458 |
B Ruaro1, A Sulli1, E Alessandri1, G Fraternali-Orcioni2, M Cutolo3.
Abstract
Kikuchi-Fujimoto's disease (KFD), or histiocytic necrotizing lymphadenitis, is a benign and self-limiting disease of unknown aetiology. KFD tends to affect a young population under 30 years of age and predominantly females. KFD is a rare pathology and its association with systemic lupus erythematosus (SLE) is not frequent. Herein, we present the case of a male Italian patient with SLE in association with KFD with 5 years of follow-up, where a differential diagnosis from infection or lymphoproliferative disease was problematic.Entities:
Keywords: Kikuchi–Fujimoto’s disease; histiocytic necrotizing lymphadenitis; systemic lupus erythematosus
Mesh:
Year: 2014 PMID: 24739458 DOI: 10.1177/0961203314530794
Source DB: PubMed Journal: Lupus ISSN: 0961-2033 Impact factor: 2.911