Results 11 to 20 of about 5,601 (170)
The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report
Journal of Medical Case Reports, 2023 Background Kikuchi–Fujimoto disease is an uncommon systemic disease that mostly affects young women. Kikuchi–Fujimoto disease typically manifests as necrotizing lymphadenopathy, which frequently follows by a fever; however, Kikuchi–Fujimoto disease ...
Maysam Yousefi +6 more
doaj +3 more sources
Indian Pediatrics Case Reports, 2021 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
core +5 more sources
Kikuchi- Fujimoto Disease of Mesenteric Lymph Nodes Mimicking Acute Appendicitis
Journal of Nepal Medical Association, 2013 Kikuchi-Fujimoto disease, or histiocytic necrotising lymphadenopathy of unknown aetiology, is a rare, benign and self-limiting cause of lymphadenopathy often involving the cervical nodes, and rarely presenting with mesenteric lymphadenopathy.
Anne Shrestha +3 more
doaj +4 more sources
Kikuchi-Fujimoto disease from eastern India
Journal of Global Infectious Diseases, 2010 Kikuchi′s disease, a rare disorder which usually presents with fever painful lymphadenopathy, rash and arthritis, all of which are close mimickers of infective and immunological disorders. It is essentially a histopathological diagnosis and tests to rule
Pankaj Singhania +4 more
doaj +2 more sources
The Kikuchi-Fujimoto Disease in Nigeria: A Case Report and Literature Review [PDF]
Case Reports in Medicine, 2014 The Kikuchi-Fujimoto is a rare, self-limiting disease, which is characterized by regional lymphadenopathy. It occurs worldwide with a higher prevalence among Asians and women below the age of forty years.
Akinsegun Akinbami +9 more
doaj +2 more sources
Kikuchi-Fujimoto Disease Associated with Symptomatic CD4 Lymphocytopenia [PDF]
Case 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 +2 more sources
Kikuchi-Fujimoto disease involving retroperitoneal lymph nodes: An uncommon presentation
Hematology Reports, 2021 Kikuchi-Fujimoto disease is a self-limited disease of unknown etiology that is clinically defined by fevers accompanied by tender posterior cervical lymphadenopathy.
Jane Date Hon +5 more
doaj +2 more sources
Kikuchi–Fujimoto disease manifesting bilateral lymphadenopathy
Clinical Case Reports, 2022 Physicians should keep in mind that Kikuchi‐Fujimoto disease can show bilateral lymphadenopathy like the present case.
Akihiro Kawatsuki +3 more
doaj +2 more sources
Medical Journal of Indonesia, 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. The most common clinical manifestation is cervical lymphadenopathy accompanied by fever, myalgia, leukopenia, and skin rash.
Soedibyo, Soepardi
openaire +4 more sources
Retinopathy in lupus transitioned to Kikuchi-Fujimoto disease
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 +2 more
doaj +2 more sources