Results 51 to 60 of about 1,749 (155)

A Case of Upper Tract Urothelial Carcinoma With Neuroendocrine Differentiation Successfully Treated With Enfortumab Vedotin and Pembrolizumab

open access: yesIJU 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

Necrotizing Histiocytic Lymphadenitis: Report of two cases (Kikuchi-Fujimoto disease)

open access: yesمجله دانشگاه علوم پزشکی گرگان, 2004
Kikuchi-Fujimoto disease is a necrotizing Lymphadenitis with benign self-limit process in young women with fever, cervical lymphadenopathy and increased ESR with leukopenia. In this report we introduce 2 females with Kikuchi-Fujimoto disease.
M.Sharbatdaran (MD)   +2 more
doaj  

Novel Clinical and Histological Insights into Cutaneous Kikuchi‐Fujimoto Disease and Kikuchi Disease‐Like Inflammatory Pattern (KLIP)

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 7, Page e983-e987, July 2026.
Magí Brufau‐Cochs   +7 more
wiley   +1 more source

Association of Immune‐Related Adverse Events and the Efficacy of Immune Checkpoint Inhibitors in Non‐Small Cell Lung Cancer: Adjusting for Immortal Time Bias

open access: yesThoracic 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

Neue klinische und histologische Erkenntnisse zur kutanen Kikuchi‐Fujimoto‐Krankheit und zum Kikuchi‐Krankheit‐ähnlichen Entzündungsmuster (KLIP)

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 7, Page 983-987, July 2026.
Magí Brufau‐Cochs   +7 more
wiley   +1 more source

Kikuchi‐Fujimoto disease: A rare case report from Nepal

open access: yesClinical Case Reports, 2021
Clinicians and pathologists must be aware of the occurrence of Kikuchi‐Fujimoto Disease, as one of the differential diagnoses of cervical lymphadenopathy.
Rahul Rauniyar   +6 more
doaj   +1 more source

Kikuchi Disease of Parotid Gland

open access: yesJBN (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

Kikuchi-Fujimoto disease: a case report and the evaluation of diagnostic procedures

open access: yesBMC 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

open access: yesCase 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

Dilemas de diagnóstico de linfadenite necrotizante (doença de Kikuchi-Fujimoto).

open access: yesActa 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

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