Results 41 to 50 of about 9,296 (170)

Kikuchi-Fujimoto disease can present as delayed lymphadenopathy after COVID-19 vaccination

open access: yesHuman Vaccines & Immunotherapeutics, 2022
Following COVID-19 vaccination, ipsilateral axillary and cervical lymphadenopathy may occur, called vaccine-related hypermetabolic lymphadenopathy, which is considered reactive lymphadenopathy.
Takeru Kashiwada   +8 more
doaj   +1 more source

Unexplained Fatigue in an Otherwise Healthy Man Linked to Kikuchi-Fujimoto Disease, A Case Report

open access: yesNepalese Medical Journal, 2021
Kikuchi histiocytic necrotizing lymphadenitis is a benign and self-limited illness usually characterized by cervical lymphadenopathy and fever. We present a case of a 42-year male who complained of extreme fatigue for 2 weeks.
Vivek Pant   +2 more
doaj   +1 more source

Clinical Abdominal Kikuchi-Fujimoto Disease Resembling Macrophage Activation Syndrome Associated with Systemic Juvenile Idiopathic Arthritis: A Case Report [PDF]

open access: yes, 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.
Ando, Yusuke   +4 more
core   +1 more source

A Case Report of Kikuchi-Fujimoto Disease with Immune Thrombocytopenic Purpura [PDF]

open access: yes, 2010
Kikuchi-Fujimoto disease (histiocytic necrotizing lymphadenitis) is a rare disease characterized by lymphadenitis with fever. It is self-limited within one to four months, and is generally diagnosed by an excisional biopsy of the affected lymph node ...
강희철, 김원용, 이승범
core   +1 more source

Kikuchi-Fujimoto Disease Associated with Symptomatic CD4 Lymphocytopenia

open access: yesCase Reports in Rheumatology, 2014
Kikuchi-Fujimoto disease is a rare benign condition of necrotising histiocytic lymphadenitis with unknown aetiology. We describe here a 30-year-old African American female who presented with fever, generalized rash, cervical lymphadenopathy, and oral ...
Meera Yogarajah, Bhradeev Sivasambu
doaj   +1 more source

Kikuchi-Fujimoto Disease in a Filipino Boy: A Case Report

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2019
Objective: To report a case of a 12-year-old boy with Necrotizing Lymphadenitis (Kikuchi-Fujimoto disease) presenting as lymphadenitis secondary to multiple diagnosis.
Jenina Rachel Escalderon, Angelo Monroy
doaj   +1 more source

Recurrent Kikuchi-Fujimoto disease

open access: yesBMJ Case Reports, 2010
We report the case of a 27-year-old, UK-born, Asian woman who suffered a rare recurrence of Kikuchi-Fujimoto disease. She presented with tender lymphadenopathy of the neck, fever and a prodrome of flu-like symptoms. She had a past medical history of biopsy-proven Kikuchi-Fujimoto disease of her right axilla 2 years earlier, which required no treatment.
Brendan Boyd, Spooner   +3 more
openaire   +3 more sources

A white man with Kikuchi-Fujimoto disease mimicking lymphoma, preceded by frequent episodes of tonsillitis: a case report [PDF]

open access: yes, 2017
BACKGROUND: Kikuchi-Fujimoto disease is a very rare cause of benign lymphadenopathy affecting mainly young Asiatic females. Little is known about the causative agent of Kikuchi-Fujimoto disease; however, there are hypotheses of infectious, autoimmune, or
Agata Szczurowska   +3 more
core   +1 more source

Retinopathy in lupus transitioned to Kikuchi-Fujimoto disease

open access: yesAmerican Journal of Ophthalmology Case Reports, 2016
Purpose: We present a patient with systemic lupus erythematosus with significant vaso-occlusive retinal findings mimicking antiphospholipid antibody syndrome, who developed Kikuchi-Fujimoto disease.
Kelly S. Rue   +2 more
doaj   +1 more source

Kikuchi Fujimoto lymphadenitis- an uncommon entity in the surgical outpatients: a case report [PDF]

open access: yes, 2017
Kikuchi Fujimoto lymphadenitis is a benign self-limiting disease with subacute necrotizing lymphadenopathy of unknown cause. The clinical, histopathological and immunohistochemical features point to viral etiology hence delaying diagnosis commonly ...
Chougle, Qurratulain   +4 more
core   +2 more sources

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