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Kikuchi-Fujimoto's Disease: A Rare and Underdiagnosed Condition with Possible Renal Involvement.
Falbo, Enrica.
Affiliation
  • Falbo E; Consultant Nephrologist at Healthbay Polyclinic Jumeirah ‒ 1-6 Al Wasl Rd ‒ Umm Al Sheif, Dubai, Emirati Arabi Uniti (UAE).
G Ital Nefrol ; 40(6)2023 Dec 22.
Article in En | MEDLINE | ID: mdl-38156536
ABSTRACT
Kikuchi-Fujimoto disease (KFD), or Histiocytic Necrotizing Lymphadenitis, is a rare disease, with worldwide distribution but is best known in Japan and South Asia. The most common feature is cervical lymphadenopathy, accompanied by tenderness or high fever, with night sweats, but it can also be asymptomatic or with a very wide range of symptoms. The diagnosis is histopathological, on excisional biopsy. The Kikuchi-Fujmoto disease can mimic lymphoma but also tuberculosis and some autoimmune diseases, or be associated with them. Nephrologists need to be aware of it, considering the potential renal involvement. The association with systemic lupus erythematosus (SLE) is the most frequent but not the only one. Early diagnosis of this disease can prevent unnecessary investigations and aggressive therapies.
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Collection: 01-internacional Database: MEDLINE Main subject: Histiocytic Necrotizing Lymphadenitis / Lupus Erythematosus, Systemic Limits: Humans Language: En Journal: G Ital Nefrol Journal subject: NEFROLOGIA Year: 2023 Document type: Article Country of publication: Italy
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Collection: 01-internacional Database: MEDLINE Main subject: Histiocytic Necrotizing Lymphadenitis / Lupus Erythematosus, Systemic Limits: Humans Language: En Journal: G Ital Nefrol Journal subject: NEFROLOGIA Year: 2023 Document type: Article Country of publication: Italy