Kikuchi-Fujimoto's disease, also called Histiocytic NecrotizingLymphadenitis is a benign, self-limited syndrome. It is a diseasemainly described in young women under 40 years of age, ithas been found in all ethnic groups and may occur in a lesserextent in men. The etiology is not known, ...
Other autoimmune diseases such as Still’s disease, Sjögren’s syndrome, polymyositis, and rheumatoid arthritis also have been reported as occurring in conjunction with KFD, albeit with less frequency than SLE [12]. KFD typically is a self-limited condition, with duration of 1 to 4 months, ...
diffuse large B-cell lymphoma [16] and hemophagocytic syndrome [17]. There are occasional reports describing cases of extranodal skin involvement or, even more rarely, of fatal
Systemic lupus erythematosus presenting with Kikuchi-Fujimoto's disease as a long-term sequela of drug-induced hypersensitivity syndrome. A possible role o... Drug-induced hypersensitivity syndrome (DIHS) is a severe form of drug eruptions associated with viral reactivations. Autoimmune diseases have ...
Autoimmune lymphoproliferative syndrome was ruled out, due to the absence of α/β double-negative T cells. Given her history suspicious for hematological disorders, bone marrow aspiration was performed, which revealed a slightly hypocellular marrow, with focal evidence of hemophagocytosis. Flow ...
The case of a man with diagnosis of Kikuchi-Fujimoto disease (KFD) and catastrophic antiphospholipid syndrome (CAPS) is reported. He presented prolonged fever, lymphadenopathies, arthralgia, weight loss, hepatosplenomegaly and positive IgM for cytomegalovirus. While he was empirically treated with tub...
Autoimmune lymphoproliferative syndrome was ruled out, due to the absence of α/β double-negative T cells. Given her history suspicious for hematological disorders, bone marrow aspiration was performed, which revealed a slightly hypocellular marrow, with focal evidence of hemophagocytosis. Flow ...
On rare occasions, a lymphadenopathic syndrome may develop, raising the clinical suspicion of a lymphoproliferative disorder. We present the case of a 30-year-old woman who developed self-limiting left axillary lymphadenopathy following COVID-19 vaccination. To date, only seven similar cases with ...
Kikuchi-Fujimoto Disease in Patients with Sjogren's Syndrome Sjogren's syndrome is a chronic autoimmune exocrinopathy associated with dry eyes and dry mouth as major clinical manifestations. It is characterized by ly... L Radfar,M Radfar,KL Moser,... - 病理学期刊(英文) 被引量: 0发表: 2013...
Nous rapportons le cas d’un syndrome myélodysplasique (SMD) présentant un LEC associé à des lésions histologiques semblables à celles d’une maladie de KF. Observation En 2009, une patiente caucasienne de 67 ans recevait le diagnostic de SMD, avec une délétion du chromosome 20 ...