Vol. 27 - Num. 106
Clinical Reviews
Sara Pons Moralesa, Jorge Funes Pérezb, Cristina Barreda Villanuevab, Pascual Barona Zamorac
aServicio de Pediatría. Hospital Universitario Doctor Peset. Valencia. España.
bMIR-Pediatría. Hospital Universitario Dr. Peset. Valencia. España.
cPediatra. CS Pare Jofré. Valencia. España.
Correspondence: S Pons. E-mail: pons.sar70@gmail.com
Reference of this article: Pons Morales S, Funes Pérez J, Barreda Villanueva C, Barona Zamora P. Kikuchi disease . Rev Pediatr Aten Primaria. 2025;27:155-9. https://doi.org/10.60147/630d790d
Published in Internet: 13-05-2025 - Visits: 1462
Abstract
Lymphadenopathy is a common reason for consultation in pediatrics. Most of the time, it is benign and self-limiting, but it can also be the initial manifestation of significant or infrequent underlying diseases. Kikuchi-Fujimoto disease, also known as non-lymphocytic histiocytic necrotizing lymphadenitis, is a rare clinical entity that mainly affects young women of Asian descent, although it has a worldwide distribution. It typically manifests with fever and lymphadenopathy, usually at the cervical level, although cases of generalized or extranodal involvement have also been described. An infectious viral or immune-mediated etiology has been proposed, and the association of Kikuchi's disease with autoimmune processes has been described, which calls for immunological monitoring of the disease after diagnosis.
Although it is a benign and self-limiting process, it is a diagnosis of exclusion based on histopathological findings that requires ruling out other diseases with a poorer prognosis that need more specific treatment.
Keywords
● Cervical lymphadenopathy ● Kikuchi disease ● Necrotizing lymphadenitis