Results 21 to 30 of about 1,477 (190)

Kikuchi-Fujimoto disease and systemic lupus erythematosus

open access: yesInternational Medical Case Reports Journal, 2016
Diego F Baenas,1 Fernando A Diehl,1 María J Haye Salinas,2 Verónica Riva,3 Ana Diller,3 Pablo A Lemos1,4 1Clinical Medicine Department, 2Rheumatology Department, 3Pathology Department, Hospital Privado Universitario de Córdoba ...
Baenas DF   +5 more
doaj   +1 more source

Laboratory diagnosis of 44 cases of pediatric histiocytic necrotizing lymphadenitis. [PDF]

open access: yesFront Pediatr
ObjectiveTo investigate the clinical features, laboratory findings, treatment, and follow-up of pediatric histiocytic necrotizing lymphadenitis (HNL) to enhance understanding of this disease.MethodsA retrospective analysis was conducted on clinical data ...
Jin J, Lu S, Lin H.
europepmc   +2 more sources

A Challenging Case of Kikuchi-Fujimoto Disease Associated with Systemic Lupus Erythematosus and Review of the Literature

open access: yesCase Reports in Hematology, 2018
Kikuchi–Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis is a rare disease that is frequently underdiagnosed due to clinical features that are similar to those of non-Hodgkin lymphomas, systemic lupus erythematosus (SLE), or infectious ...
Mihaela Găman   +8 more
doaj   +2 more sources

Kikuchi's Disease: A Rare Cause of Fever and Lymphadenopathy

open access: yesClinical Medicine Insights: Pathology, 2012
Kikuchi's disease is a benign condition that occurs in women. A young woman presented to the hospital with fevers and cervical lymphadenopathy. Infectious work-up was negative except for streptococcus pharyngitis. Imaging studies revealed the presence of
A Vivekanandarajah   +3 more
doaj   +2 more sources

Report of a rare case of histiocytic necrotizing lymphadenitis with bilateral pleural effusion diagnosed via cervical lymph node biopsy. [PDF]

open access: yesSao Paulo Med J, 2018
CONTEXT: Histiocytic necrotizing lymphadenitis (HNL) is a rare disorder that is often benign and self-limiting. There have been reports of co-occurrence of HNL with other diseases, including systemic lupus erythematosus, hemophagocytic syndrome and ...
Liu X, Huang S, Jiang G.
europepmc   +2 more sources

Histiocytic necrotizing lymphadenitis with hemophagocytic lymphohistiocytosis in adults: A single-center analysis of 5 cases. [PDF]

open access: yesImmun Inflamm Dis
Background Histiocytic necrotizing lymphadenitis (HNL) is a self‐limited inflammatory disease of unknown pathogenesis. A very small fraction of patients with HNL could develop hemophagocytic lymphohistiocytosis (HLH), a hyperinflammatory disorder.
Chen Q   +10 more
europepmc   +2 more sources

Localised Kikuchi-Fujimoto Disease With Mediastinal Lymphadenopathy: A Case Initially Mimicking Malignant Lymphoma on Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration Cytology. [PDF]

open access: yesRespirol Case Rep
We report a rare case of isolated mediastinal Kikuchi–Fujimoto disease (KFD) in a 37‐year‐old woman, which was initially misinterpreted as malignant lymphoma based on EBUS‐TBNA cytology. Definitive diagnosis was achieved through video‐assisted thoracoscopic surgery, revealing characteristic massive necrosis and histiocytic infiltration.
Nishiyama K   +10 more
europepmc   +2 more sources

Serum Cytokine Profiling Differentiates Underlying Diseases in Cytokine Storm Syndrome. [PDF]

open access: yesArthritis Rheumatol
Serum cytokine profiling was performed using Luminex (48 cytokines) and ELISA (5 cytokines). Assessment of key cytokines (IFN‐α, IL‐18, IL‐6, CXCL9) delineated five dominant inflammatory patterns: I, IFN‐α–dominant CSS; II, IL‐18–dominant CSS; III, IL‐6–dominant CSS; IV, IFN‐γ–dominant CSS; and V, IL‐6 & IFN‐γ intermediate CSS.
Kaneko S   +42 more
europepmc   +2 more sources

Case Report: Kikuchi-Fujimoto Disease: A case of supraclavicular lymphadenopathy [version 2; peer review: 2 approved]

open access: yesF1000Research, 2021
Kikuchi-Fujimoto Disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare cause of cervical lymphadenopathy. Patients usually present with localized lymphadenopathy, fever and fatigue.
Shiza Sarfraz   +3 more
doaj   +1 more source

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