Results 21 to 30 of about 9,296 (170)
Kikuchi-Fujimoto disease [PDF]
![Figure][1] A 20-year-old man presented with a 3-week history of fevers, night sweats, weight loss, and increasing cervical adenopathy. A comprehensive infectious disease workup was negative.
Branko, Cuglievan, Roberto N, Miranda
+5 more sources
Kikuchi-Fujimoto disease: investigating comprehensive clinicopathological features and risk factors for recurrence. [PDF]
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.
Nishimura MF +6 more
europepmc +2 more sources
Background: Kikuchi Fujimoto disease (KFD) is a rare, benign self-limited disease characterized by prolonged regional lymphadenopathy associated with or without systemic signs or symptoms. It is a rare diagnosis in children.
Sangeeta Priyadarshi Sawant +3 more
openaire +4 more sources
Kikuchi–Fujimoto disease: literature review and report of four cases
Kikuchi–Fujimoto disease, or necrotizing histiocytic lymphadenitis, is one of the rare causes of benign lymphadeno-pathy. The diagnosis is based on histological and immunohistochemical analysis of the lymph node biopsy. The article presents four clinical
V. G. Potapenko +5 more
doaj +1 more source
Kikuchi-Fujimoto disease. [PDF]
A 14 year-old Bangladeshi girl presented with high fever, painful swellings in the neck, anorexia, weight loss and night sweating. On examination she had multiple enlarged and tender cervical lymph nodes. Other systems were normal. Laboratory investigations for sepsis and autoimmune diseases were negative. Initial fine needle aspiration and cytology of
R, Parveen +5 more
+9 more sources
Abstract Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a self-limited condition, characterized by benign lymphadenopathy with associated fevers and systemic symptoms. It most commonly affects adults younger than 40 years of age and of Asian descent. Involved lymph nodes demonstrate paracortical areas of apoptotic
Charles Blake, Hutchinson, Endi, Wang
openaire +4 more sources
Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report
Background We present a yet to be described association of SARS-CoV-2 infection with Kikuchi-Fujimoto disease. Case presentation A 32-year-old physician with history of SARS-CoV-2 infection presented to the emergency department with 2 weeks of fever ...
Samuel D. Racette +7 more
doaj +1 more source
Serum Alkaline Phosphatase Levels in Pediatric Kikuchi-Fujimoto Disease: A Retrospective Observational Analysis. [PDF]
The diagnosis of Kikuchi‐Fujimoto disease remains challenging and often requires invasive biopsy. Serum alkaline phosphatase levels were < 50% of the age‐ and sex‐specific median values in patients with Kikuchi‐Fujimoto's disease. Decreased serum alkaline phosphatase levels, mainly when assessed as a percentage of age‐ and sex‐specific reference ...
Fujiwara S, Higuchi Y, Shimizu J.
europepmc +2 more sources
Kikuchi Disease with enlargement of intramammary lymph node
We describe a rare case of intramammary lymphadenopathy due to Kikuchi-Fujimoto disease. A 15-year old female presented to the Breast Clinic with complaints of a tender, palpable right breast lump.
Michael A Simon, MD +4 more
doaj +1 more source
Kikuchi-Fujimoto disease following SARS CoV2 vaccination: Case report
Kikuchi's disease (KD) also known as Kikuchi-Fujimoto disease (KFD), or histiocytic necrotizing lymphadenitis was first described in 1972 independently by Kikuchi and Fujimoto et al. It is a benign self-limited condition of unknown etiology which usually
Hussam Al Soub +5 more
doaj +1 more source

