Results 51 to 60 of about 5,601 (170)
Kikuchi-Fujimoto disease and COVID-19. Case report
, 2021 Introducción: la enfermedad de Kikuchi-Fujimoto se considera una linfadenitis necrosante histiocitaria de infrecuente presentación. Su diagnóstico es anatomopatológico.
Artiles Martínez, Daniel +2 more
core +1 more source
ChemBioChem, Volume 27, Issue 5, 13 March 2026.The glycolipid‐peptide antigen complexes for self‐adjuvanting conjugates were successfully synthesized, and, with the HLA‐transgenic mice, the antigen‐specific CD8+ T cell expansion was exhibited. The results provide useful insights for the design and synthesis of vaccine conjugates using glycolipid antigen as an adjuvant.
Shunya Kikuchi +4 more
wiley +1 more source
IJU Case Reports, Volume 9, Issue 2, March 2026.ABSTRACT Introduction Upper tract urothelial carcinoma with neuroendocrine differentiation (UC‐NE) is extremely rare and generally associated with aggressive behavior and poor prognosis. Optimal treatment strategies remain unclear, particularly regarding the role of nectin‐4–targeted therapy. Case Presentation A 61‐year‐old man was diagnosed with UC‐NE
Kosei Taniguchi +9 more
wiley +1 more source
Thoracic Cancer, Volume 17, Issue 6, March 2026.Immortal time bias (ITB)–adjusted landmark and time‐dependent Cox analyses showed that immune‐related adverse events (irAEs) were not associated with improved survival in NSCLC patients receiving first‐line immune checkpoint inhibitors. ECOG performance status remained the key prognostic factor.
Yoshiki Kuwabara +20 more
wiley +1 more source
Journal of Diabetes Investigation, Volume 17, Issue 6, Page 901-904, June 2026.
wiley +3 more sources
Kikuchi-Fujimoto disease [PDF]
La Revue de medecine interne, 2011 Kikuchi-Fujimoto disease is a necrotizing lymphadenitis, involving young patients, predominantly females. Lymphadenopathy is usually localized, particularly in the cervical area, mostly unilateral and tender. Fever is present in one third of cases. Associated skin lesions, arthralgia, myalgia, splenomegaly or hepatomegaly are rare.
openaire +3 more sources
Kikuchi-Fujimoto disease: a case report and the evaluation of diagnostic procedures
BMC Oral Health, 2019 Background Kikuchi-Fujimoto disease, known as histiocytic necrotizing lymphadenitis, is a benign, self-limiting and systemic disorder involving lymph nodes with unknown aetiology.
Shenjie Xu, Weilian Sun, Jiamei Liu
doaj +1 more source
Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report
Case Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.Kikuchi–Fujimoto Disease (KFD) is a rare, typically self‐limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small‐vessel vasculitis. Central nervous system (CNS) involvement in KFD is exceedingly rare and has been described in isolated cases, including encephalitis, aseptic meningitis, and ...
Yusuf Kagzi +5 more
wiley +1 more source
Kikuchi Disease of Parotid Gland
JBN (Jurnal Bedah Nasional)Aim: Kikuchi disease, often referred to as Kikuchi–Fujimoto disease (KFD), is an uncommon benign cervical lymphadenitis etiology. Cervical lymphadenopathy is Kikuchi disease's most prevalent clinical sign.
William Stevenson +2 more
doaj +1 more source
Dilemas de diagnóstico de linfadenite necrotizante (doença de Kikuchi-Fujimoto).
Acta Médica Portuguesa, 2011 Kikuchi-Fujimoto disease, also called Histiocytic necrotizing lymphadentis, is a rare, benign and self-limited disease, with unknown etiology, that affects mainly young women, and is characterized by adenopathy (usually localized in the cervical region ...
Inês Antunes +8 more
doaj +1 more source