Results 81 to 90 of about 9,296 (170)
The Septuagenarian, Octogenarian, Nonagenarian Investigation with Centenarian (SONIC) study was established considering population trends and targeting the oldest‐old population. This study is unique in its narrow age range, consisting of individuals aged in their 70s, 80s and 90s, and is carried out as a longitudinal cohort study with follow ups every
Kei Kamide +153 more
wiley +1 more source
Kikuchi–Fujimoto Disease Presenting as Brachial Plexus Neuritis: A Case Report
Kikuchi–Fujimoto disease is a rare, idiopathic, self-limiting necrotizing lymphadenitis of unknown etiology. It usually affects young Asian women. Clinically, it closely resembles with tuberculosis or lymphomas.
Rakesh Gupta +2 more
doaj +1 more source
Association of IL-10 receptor 2 (IL10RB) SNP with systemic sclerosis [PDF]
Interleukin-10 (IL-10) signaling has been suggested to play a role in systemic sclerosis (SSc). IL10RB codes for IL-10 receptor 2 (IL-10R2), a component shared in receptor complexes for IL-10, IL-22, IL-26 and interferon (IFN)-λ.
Ehara Yukikazu +10 more
core +1 more source
The Journal of Dermatology, Volume 52, Issue 6, Page e430-e480, June 2025.
Yoshihide Asano +27 more
wiley +1 more source
Kikuchi–Fujimoto Disease in a Young Male with Fever Postvascular Surgery
Kikuchi–Fujimoto disease is a rare self-limiting necrotizing lymphadenitis usually affecting young adults. It commonly presents with tender posterior cervical lymphadenopathy and fever.
Rahul Kumar +4 more
doaj +1 more source
A Case of Relapsing Kikuchi-Fujimoto Disease [PDF]
Kikuchi-Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis was first described in Japan in 1972. It is described as a benign syndrome most commonly involving cervical lymphadenopathy, fever, and night sweats.
Carroll, Matthew B. +3 more
core +2 more sources
Kikuchi-Fujimoto disease in 21-year-old man
Kikuchi-Fujimoto disease also known as histiocytic necrotizing lymphadenitis is a benign disorder characterized histologically by necrotic foci surrounded by histiocytic aggregates, and with the absence of neutrophils.
Saeid Aminiafshar +2 more
doaj
The evaluation of pediatric neck masses offers the opportunity for consideration of a diverse range of pathologies, from infectious to neoplastic. A 16-year-old female presented with 2 weeks of worsening swelling and pain of a left-sided neck mass ...
Joseph Burns +6 more
doaj +1 more source
Cross-disease innate gene signature: Emerging diversity and abundance in RA comparing to SLE and SSc [PDF]
Overactivation of the innate immune system together with the impaired downstream pathway of type I interferon-responding genes is a hallmark of rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and systemic sclerosis (SSc).
Fillerová, Regina +8 more
core +1 more source
Apresentação de um caso de febre de origem obscura numa paciente feminina de 35 anos, com queda do estado geral, adenomegalia cervical posterior, monilíase oral, parotidite e irite.Após o parecer oftalmológico, o tratamento foi iniciado e posteriormente ...
Marco Aurelio Varella Figueiredo +2 more
doaj +1 more source

