Results 51 to 60 of about 1,477 (190)

Unveiling the Molecular Landscape of MPO in Kikuchi's Disease: Protein Expression, mRNA Levels, and Genetic Polymorphisms

open access: yesInternational Journal of Laboratory Hematology, Volume 47, Issue 5, Page 898-905, October 2025.
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

Supplementary Material for: Treating Histiocytic Necrotizing Lymphadenitis with Chinese Herbs: A Case Report

open access: yes, 2017
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

open access: yesIndian Journal of Dermatology, 2016
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

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‐Fujimoto disease: investigating comprehensive clinicopathological features and risk factors for recurrence

open access: yesHistopathology, Volume 87, Issue 1, Page 68-80, July 2025.
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

open access: yesTurkish Archives of Otorhinolaryngology, 2013
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

open access: yesArchives of Academic Emergency Medicine, 2018
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

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

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

Systemic Inflammatory Diseases in Children With Sickle Cell Disease: A French Multicenter Observational Study on Diagnostic and Therapeutic Issues

open access: yesPediatric Blood &Cancer, Volume 72, Issue 4, April 2025.
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

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