Results 41 to 50 of about 4,944,354 (189)
Kikuchi-Fujimoto disease associated optic neuropathy in an adolescent. [PDF]
Am J Ophthalmol Case RepPurpose We present a case of Kikuchi-Fujimoto Disease (KFD) associated with bilateral optic neuropathy progressing to vision loss. Observations A 17-year-old male was referred for bilateral optic nerve pallor. Eight years prior, he was diagnosed with KFD
Cheong JH, Nayer Z, Odel JG.
europepmc +2 more sources
Management of Kikuchi-Fujimoto Disease Using Glucocorticoid: A Case Report [PDF]
Case Reports in Medicine, 2011 Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis, is a self-limiting, benign, and rare systemic lymphadenitis with unknown etiology.
Selim Yalcin +5 more
doaj +2 more sources
Kikuchi-Fujimoto disease [PDF]
The Lancet, 2014 In February, 2013, a 30-year-old Ugandan-born woman, working in the UK, presented to the accident and emergency department with a 4-week history of arthralgia, fevers, and lethargy, and a recent episode of possible tonsillitis. During the third week of symptoms, she developed epistaxis, periorbital swelling, and rash.
Julian, Dalton +2 more
+6 more sources
Kikuchi-Fujimoto disease [PDF]
Blood, 2017 ![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: A Case Report
Turkish Archives of Otorhinolaryngology, 2003 Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is a disease often presents with fever, malaise, and lymphadenopathy primarily involving the cervical lymph nodes, found mainly in young women.
Emin Karaman +5 more
doaj +4 more sources
A very rare localization of kikuchi-fujimoto disease: parotid gland
B-ENT, 2020 Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is a rare benign disorder characterized by necrotizing lymphadenitis, which was independently defined by Kikuchi and Fujimoto in 1972.
Mehmet Özgür Pınarbaşlı +4 more
doaj +3 more sources
Clinical Abdominal Kikuchi-Fujimoto Disease Resembling Macrophage Activation Syndrome Associated with Systemic Juvenile Idiopathic Arthritis: A Case Report [PDF]
, 2022 A 13-year-old girl presented with fever for the past ten days without any other symptoms. Laboratory findings revealed leukopenia, low platelet count, and high lactate dehydrogenase and ferritin levels.
Fujita, Yuji +4 more
core +1 more source
Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report
BMC Infectious Diseases, 2021 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
Archives of Pathology & Laboratory Medicine, 2010 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.
Charles Blake, Hutchinson, Endi, Wang
openaire +4 more sources
Kikuchi Disease with enlargement of intramammary lymph node
Radiology Case Reports, 2021 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