Kikuchi-Fujimoto disease: a rare but important differential diagnosis for lymphadenopathy.

BMJ Case Rep

Department of Haematology, Centre of Clinical Haematology, Queen Elizabeth Hospital, Birmingham, UK.

Published: September 2014

A 23-year-old man presented with a 6-week history of fevers, cervical lymphadenopathy and fatigue. A CT of the neck, chest, abdomen and pelvis showed left cervical lymphadenopathy, enlarged lymph nodes in the axilla and groin and hepatomegaly. A left cervical excisional lymph node biopsy was undertaken and the histopathological findings were consistent with Kikuchi-Fujimoto disease. He was treated with high-dose prednisolone for 1 week, which was then tapered. Generalised arthralgia and daily episodes of malaise were experienced for a subsequent 2 months following the cessation of corticosteroids. The condition lasted 4 months from the onset of symptoms. This case report highlights the importance of including Kikuchi-Fujimoto disease as a differential diagnosis for lymphadenopathy. Kikuchi-Fujimoto disease has commonly been mistaken for tuberculosis and lymphoma, and unnecessary exposure to agents used to treat these conditions can be avoided by prompt histological diagnosis.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158208PMC
http://dx.doi.org/10.1136/bcr-2014-205470DOI Listing

Publication Analysis

Top Keywords

kikuchi-fujimoto disease
16
differential diagnosis
8
diagnosis lymphadenopathy
8
cervical lymphadenopathy
8
left cervical
8
kikuchi-fujimoto
4
disease rare
4
rare differential
4
lymphadenopathy
4
lymphadenopathy 23-year-old
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!