Results 51 to 60 of about 1,477 (190)
This study investigates myeloperoxidase (MPO) in Kikuchi's disease, analyzing protein expression and mRNA levels in 43 patients. Results reveal 100% MPO protein positivity, elevated mRNA expression, and a positive correlation between mRNA and protein levels.
Chen Chang +4 more
wiley +1 more source
We present the case of a young woman who suffered from right cervical lymphadenopathy with associated malaise for 8 weeks. The sonography showed multiple, enlarged lymph nodes in the cervical, submaxillary, and subclavicular chains on the right side. The
Zhou J. (3931118) +5 more
core +1 more source
Kikuchi-fujimoto disease, the masquerading menace: A rare case report
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
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
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 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
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
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
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
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

