Kikuchi-Fujimoto disease: A study of Four cases

Kikuchi-Fujimoto disease (KFD) manifests in most cases as unilateral cervical lymphadenomegaly with or without accompanying fever. The disease is rare and mainly affects young women and has a self-limited course. KFD should be included in the differential diagnosis of suspected cases of viral i...

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Bibliographic Details
Main Author: Abhijeet Ingle1 , Vijaya Gattu2 , Suhela R3
Format: Article
Language:English
Published: Prathima Institute of Medical Sciences 2017-08-01
Series:Perspectives In Medical Research
Subjects:
Online Access:http://www.pimr.org.in/Ingle-vol-5-issue-2.PDF
Description
Summary:Kikuchi-Fujimoto disease (KFD) manifests in most cases as unilateral cervical lymphadenomegaly with or without accompanying fever. The disease is rare and mainly affects young women and has a self-limited course. KFD should be included in the differential diagnosis of suspected cases of viral infections, tuberculosis, reactive lymphadenitis, systemic lupus erythematosus and metastatic diseases. It can be histologically confused with lymphoma. The disease is benign and selflimiting and an excisional biopsy of an affected lymph node is often necessary for diagnosis. There is no specific therapy. This study reports four cases of female patients with KFD who were attended at Yashoda hospital, Malakpet. A review of the literature was carried out with a systematic search on this topic with the aim of informing physicians about this entity that is manifested by cervical masses and fever. Fourth case was interesting because of its association with autoimmune disease (SLE-systemic lupus erythematosus
ISSN:2348-1447
2348-229X