Kikuchi-Fujimoto disease: A case report

1Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.

Abstract

Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is an idiopathic, self-limiting disorder and predominantly affects young women. We report a 35-year-old female who presented with soft to firm cervical lymphadenopathy and neck pain. She had multiple enlarged cervical nodes. Examination of other systems was normal. Lymph node biopsy was performed, and the histological features, and immunohistochemistry confirmed the diagnosis. The Patient was treated with non-steroidal anti-inflammatory drugs and low-dose prednisolone. A significant decrease in the size of lymph node and relief of neck pain occurred. During four years of follow-up, the patient developed no malignant disease or systemic and autoimmune diseases such as systemic lupus erythematosus. Kikuchi-Fujimoto disease is rare, clinicians should be aware of this condition as early diagnosis of the disease will lessen concerns of the patient's family.

Cite

CITATION STYLE

APA

Aznab, M., Kamalian, N., Navabi, J., & Kavianimoghadam, K. (2015). Kikuchi-Fujimoto disease: A case report. Acta Medica Iranica, 53(11), 725–727. https://doi.org/10.3329/bjch.v34i3.10362

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free