Results 81 to 90 of about 3,532 (210)
Medicover Journal of MedicineKikuchi–Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare disease first reported in 1972 by Kikuchi and Fujimoto et al. It is more common in young females under 30 years of age.
Sudarshan Pandit +5 more
semanticscholar +1 more source
Histopathology, Volume 87, Issue 1, Page 68-80, July 2025.Comprehensive clinicopathological analysis of 112 cases of Kikuchi‐Fujimoto disease (KFD) was conducted, and offered insights into recurrence risk factors and histopathological patterns. Recurrent KFD may fall between transient KFD and overt autoimmune disorders and lead to a better understanding of the aetiology of KFD.
Midori Filiz Nishimura +6 more
wiley +1 more source
Kikuchi-Fujimoto disease in a young patient : a case report [PDF]
, 2022 A rare form of lymphadenopathy called Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, was discovered in Japan in 1972 by Kikuchi and Fujimoto.
Wan Ramli, Wan Nurliyana +5 more
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Kikuchi-fujimoto disease, the masquerading menace: A rare case report
Indian Journal of Dermatology, 2016 Kikuchi-Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis is a rare, benign, self-limiting disease with unknown etiology characterized by regional lymphadenopathy.
Rohit Kataria +5 more
doaj +1 more source
Subacute Mastoiditis Without Verified Nontuberculous Mycobacteria—Still a Clinical Challenge
Laryngoscope Investigative Otolaryngology, Volume 10, Issue 3, June 2025.SAM represents an indolent form of mastoiditis with potential serious complications. Radiology, histopathological, and microbiological sampling is crucial for diagnosing this infection to optimize treatment and improve outcome. ABSTRACT Objective An indolent form of mastoiditis has gained increased attention lately, challenging clinicians both ...
Lara Kakabas +3 more
wiley +1 more source
Pediatric Rheumatology Online JournalBACKGROUND Histiocytic necrotizing lymphadenitis (HNL) is a benign condition in children that is often misdiagnosed due to its clinical overlap with tuberculosis, rheumatic diseases, and lymphadenitis.
Qing Wang +5 more
semanticscholar +1 more source
Clinical and Experimental Neuroimmunology, Volume 16, Issue 2, Page 174-187, May 2025.ABSTRACT Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy (GFAP‐A) is an autoimmune inflammatory central nervous system disease. Recent neuropathological findings indicate that GFAP‐specific cluster of differentiation (CD)8+ T cells are likely the effectors of GFAP‐A.
Akio Kimura
wiley +1 more source
Turkish Archives of Otorhinolaryngology, 2013 Kikuchi Fujimato disease (KFD) also know as histiocytic necrotizing lymphadenitis (HNL) is a benign, self limiting disease, which commonly affects young women under 30 years of age. Most of the cases resolve in a six month period. Laboratory and clinical
Burak Ertaş +4 more
doaj +1 more source
Kikuchi-Fujimoto Disease in an Iranian Woman; a Rare but Important Cause of Lymphadenopathy
Archives of Academic Emergency Medicine, 2018 Kikuchi-Fujimoto Disease (KFD), is a rare and self-limited condition of histiocytic necrotizing lymphadenitis, which typically presents as fever and lymphadenopathy. We describe a case of KFD in an Iranian woman. Due to low incidence and high importance,
Mana Baziboroun +4 more
doaj +1 more source
Pediatric Blood &Cancer, Volume 72, Issue 4, April 2025.ABSTRACT Background Systemic inflammatory diseases (SIDs) have been reported in patients with sickle cell disease (SCD), but clinical data in children are scarce. Objectives To identify clinical and laboratory features at diagnosis of SID in children with SCD and to describe their evolution.
Caroline Vinit +19 more
wiley +1 more source