Results 21 to 30 of about 4,930,328 (151)

Retinopathy in lupus transitioned to Kikuchi-Fujimoto disease [PDF]

American 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, Damien C. Rodger, Narsing A. Rao   +2 more
doaj   +2 more sources

Kikuchi-Fujimoto Disease Associated with Myasthenia Gravis: A Case Report [PDF]

Case Reports in Medicine, 2010
Kikuchi-Fujimoto disease is a self-limited benign condition of unknown etiology characterized by cervical lymphadenopathy, fever, and leucopenia. An autoimmune hypothesis has been suggested and an association with systemic lupus erythematosus, Sjogren's ...
Olukayode Onasanya, David Nochlin, Victor Casas, Leema Reddy Peddareddygari, Raji P. Grewal   +4 more
doaj   +2 more sources

Kikuchi-Fujimoto disease in 21-year-old man

International Journal of Preventive Medicine, 2013
Kikuchi-Fujimoto disease also known as histiocytic necrotizing lymphadenitis is a benign disorder characterized histologically by necrotic foci surrounded by histiocytic aggregates, and with the absence of neutrophils.
Saeid Aminiafshar, Najmeh Namazi, Farhad Abbasi   +2 more
doaj   +1 more source

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, Selami Kocak Toprak, Betul Erismis, Ozden Altundag, Handan Ozdemir, Nuray Topcuoglu   +5 more
doaj   +2 more sources

Kikuchi-Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report. [PDF]

Case Rep Neurol Med
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 ...
Kagzi Y, Amatya S, Gupta A, Sharma K, Sriwastava S.   +4 more
europepmc   +2 more sources

Novel Clinical and Histological Insights into Cutaneous Kikuchi-Fujimoto Disease and Kikuchi Disease-Like Inflammatory Pattern (KLIP). [PDF]

J Dtsch Dermatol Ges
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 7, Page e983-e987, July 2026.
Brufau-Cochs M, Bosch-Amate X, Gil-Lianes J, de Anta NC, Iranzo P, Giavedoni P, García-Herrera A, Mascaró JM.   +7 more
europepmc   +2 more sources

Negative Correlation Between Serum Ferritin and CD4+ Lymphocytes: A Retrospective Study on Kikuchi-Fujimoto Disease. [PDF]

Immun Inflamm Dis
This retrospective cohort study indicates that patients with Kikuchi–Fujimoto disease demonstrated immunosuppression characterized by decreased counts of circulating CD3+ and CD4+ lymphocytes. Moreover, serum ferritin levels were inversely correlated with CD4+ lymphocyte counts, suggesting a potential role of ferritin in immune dysregulation in Kikuchi–
Zhong P, Sang X, Yang Y, Wang Z.
europepmc   +2 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, Yoshihara, Shigemi, Kuwashima, Shigeko, Ando, Yusuke, Kato, Tamae   +4 more
core   +1 more source

Localised Kikuchi-Fujimoto Disease With Mediastinal Lymphadenopathy: A Case Initially Mimicking Malignant Lymphoma on Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration Cytology. [PDF]

Respirol Case Rep
We report a rare case of isolated mediastinal Kikuchi–Fujimoto disease (KFD) in a 37‐year‐old woman, which was initially misinterpreted as malignant lymphoma based on EBUS‐TBNA cytology. Definitive diagnosis was achieved through video‐assisted thoracoscopic surgery, revealing characteristic massive necrosis and histiocytic infiltration.
Nishiyama K, Hasegawa T, Ishimine T, Nagae R, Shimabukuro T, Nishiyama M, Fukuzato N, Murayama Y, Tamaki K, Kakazu O, Ohta M.   +10 more
europepmc   +2 more sources

Kikuchi-Fujimoto Disease [PDF]

, 2005
Kikuchi-Fujintoto disease (KFD) was first reported by 2 Japanese pathologists, Kikuchi and Fujimoto, independently in 1972. KFD is an idiopathic, self-limited necrotizing lymphadenitis.
Soedibyo, Soepardi
core   +1 more source