| Literature DB >> 25564582 |
Santosh Nagaraju1, Sakshi Vaishnav2, Leandra H Burke2, Earl M Norman2.
Abstract
Kikuchi-Fujimoto disease (KFD) or histiocytic necrotising lymphadenitis is a rare entity, occurring most commonly in young Asian adults. KFD is characterised by fever with tender lymph node enlargement. The cervical group of lymph nodes is most commonly involved, and the diagnosis is conclusively made by lymph node biopsy and histopathology. KFD is a self-limiting condition, which usually resolves over 1-4 months. Symptomatic treatment with antipyretics and/or non-steroidal anti-inflammatory drugs is recommended. Here we describe an uncommon presentation of KFD in a young woman in which only the axillary lymph nodes were enlarged. 2015 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2015 PMID: 25564582 PMCID: PMC4289788 DOI: 10.1136/bcr-2014-203776
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X