Results 61 to 70 of about 2,190 (225)

Kikuchi-Fujimoto Disease Associated with Myasthenia Gravis: A Case Report [PDF]

open access: yes, 2010
Kikuchi-Fujimoto disease is a self-limited benign condition of unknown etiology characterized by cervical lymphadenopathy, fever, and leucopenia. An autoimmune hypothesis has been suggested and an association with systemic lupus erythematosus, Sjogren's ...
Casas, Victor   +4 more
core   +3 more sources

Comparison of Clinical Characteristics and Risk Factors for Recurrence of Kikuchi-Fujimoto Disease Between Children and Adult [PDF]

open access: yes, 2022
Purpose: Kikuchi-Fujimoto disease (KFD) is a rare, benign, and self-limited disease, characterized by cervical lymphadenopathy and fever. Herein, we analyzed the differences in its clinical manifestations and risk factors for recurrence between children ...
강지만, 안종균
core   +1 more source

Fibrosing Mediastinitis in a 5‐Year‐Old Labrador Retriever

open access: yesVeterinary Medicine and Science, Volume 11, Issue 4, July 2025.
This case report describes the first documented instance of fibrosing mediastinitis in a dog, characterized by chronic cough, progressive aphonia, pleural effusion and cranial vena caval syndrome. Advanced imaging revealed a soft tissue‐dense mediastinal mass, and histopathology confirmed dense fibrous tissue with chronic inflammation and vasculitis ...
Kyle L. Granger Jr.   +5 more
wiley   +1 more source

Kikuchi´s disease of the xanthomathous type with cutaneous manifestation [PDF]

open access: yes, 2015
Kikuchi's disease is a benign, self-limiting disease, whose pathogenesis remains unknown. Patients most often present with cervical lymphadenopathy, sometimes associated with fever and leukopenia.
Araújo, C   +4 more
core   +2 more sources

Rare Association between Kikuchi's Disease and Systemic Lupus Erythematosus [PDF]

open access: yesIranian Journal of Medical Sciences, 2009
Histiocytic necrotizing lymphadenitis or Kikuchi's disease is arare, benign condition of unknown etiology, which is usuallycharacterized by cervical lymphadenopathy and fever.
Mohammadhassan Jokar   +2 more
doaj  

Is recurrent Kikuchi-Fujimoto disease a precursor to systemic lupus erythematosus?

open access: yesRomanian Journal of Internal Medicine, 2019
Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare, benign, self-limiting disease characterized by cervical lymphadenopathy and fever.
Horino Taro, Ichii Osamu, Terada Yoshio
doaj   +1 more source

Kikuchi Fujimoto disease associated with cryptogenic organizing pneumonia: case report and literature review [PDF]

open access: yes, 2010
Background The association of Kikuchi Fujimoto disease (KFD) with cryptogenic organizing pneumonia (COP) is extremely rare. We report a case of simultaneous diagnosis of KFD and COP.
AU Wells   +16 more
core   +3 more sources

Subacute Mastoiditis Without Verified Nontuberculous Mycobacteria—Still a Clinical Challenge

open access: yesLaryngoscope 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

Identification of novel single nucleotide polymorphism (SNP) in DPB1 gene in ethnic population from West Bengal [PDF]

open access: yes, 2011
HLA-DP antigens present peptides to CD4+ T cells and play an important role in autoimmune diseases and parasitic infections. We have sequenced HLA-DPB1 exon-2 from the ethnic populations in West Bengal, India and report a novel single nucleotide ...
Pramanik Lucy   +4 more
core   +1 more source

Clinical and Radiological Advances in Autoimmune GFAP Astrocytopathy: Analysis of 387 Patients in Japan

open access: yesClinical 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

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