Results 71 to 80 of about 8,209 (172)
Necrotizing Histiocytic Lymphadenitis: Report of two cases (Kikuchi-Fujimoto disease)
مجله دانشگاه علوم پزشکی گرگان, 2004 Kikuchi-Fujimoto disease is a necrotizing Lymphadenitis with benign self-limit process in young women with fever, cervical lymphadenopathy and increased ESR with leukopenia. In this report we introduce 2 females with Kikuchi-Fujimoto disease.
M.Sharbatdaran (MD) +2 more
doaj
Familial Kikuchi-Fujimoto disease [PDF]
Journal of Clinical and Scientific Research, 2015 Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting disease of unknown aetiology presenting with cervical lymphadenopathy, fever, vomiting, weight loss, night sweats and chills. Familial occurrence of KFD is reported very rarely in literature.
Krishnappa J +3 more
doaj +1 more source
Enigmatic Kikuchi-Fujimoto Disease A Comprehensive Review [PDF]
American Journal of Clinical Pathology, 2004 To determine the clinicopathologic significance of Kikuchi-Fujimoto disease (KFD) and review the literature on this condition, we conducted a MEDLINE search of English-language articles published between 1972 and December 2003. KFD has a worldwide distribution, and Asiatic people have a higher prevalence.
Xavier, Bosch +3 more
openaire +2 more sources
A Case of Relapsing Kikuchi-Fujimoto Disease [PDF]
, 2013 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: an unusual association with acute renal failure
Brazilian Journal of Infectious Diseases, 2010 Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis of unknown etiopathogenesis, is a self-limited disease which frequently appears as feverish lymphadenomegaly, thus creating the need for differential diagnosis with lymphoma ...
Amanda Feliciano da Silva, MD +4 more
doaj +1 more source
Cross-disease innate gene signature: Emerging diversity and abundance in RA comparing to SLE and SSc [PDF]
, 2019 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
Acta Médica Portuguesa, 2005 Kikuchi and Fujimoto's disease, also known as histiocytic necrotizing lymphadenopathy, is a rare and benign disorder of the lymph nodes of young adults.
Alice Reichert +4 more
doaj +1 more source
Heterozygous germline TET2 loss‐of‐function variants associated with an ALPS‐like phenotype
British Journal of Haematology, Volume 206, Issue 5, Page 1330-1334, May 2025.Summary Germline homozygous loss‐of‐function mutations in TET2 result in significant childhood immunodeficiency that resembles autoimmune lymphoproliferative syndrome and predisposes one to lymphoma. The implications of heterozygous variants are less well understood.
Sean Harrop +13 more
wiley +1 more source
Insufficient control of blood pressure and incident diabetes [PDF]
, 2009 OBJECTIVE: Incidence of type 2 diabetes might be associated with preexisting hypertension. There is no information on whether incident diabetes is predicted by blood pressure control.
CHINALI, MARCELLO +8 more
core +1 more source
Kikuchi–Fujimoto Disease Presenting as Brachial Plexus Neuritis: A Case Report
Indian Journal of Neurosurgery, 2016 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