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

