| Literature DB >> 32843398 |
Laura Cannon1, Endi Wang2, Mara Becker3.
Abstract
Kikuchi-Fujimoto disease (KFD) is a rare lymphohistiocytic disorder which can cause prolonged fever and other systemic B symptoms including diffuse lymphadenopathy. Given its clinical presentation, there is often initial concern for lymphoma and diagnosis requires lymph node biopsy. It most frequently affects young women of Asian descent; it is less commonly encountered in paediatric patients. KFD is typically a benign, self-limited process, however, there is an association with development of systemic lupus erythematosus. Given its rarity, it remains unclear if KFD is associated with other chronic conditions. Here we present the third case of KFD occurring in a paediatric patient with sickle cell disease. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: paediatrics; rheumatology; sickle cell disease; systemic lupus erythematosus
Mesh:
Year: 2020 PMID: 32843398 PMCID: PMC7449481 DOI: 10.1136/bcr-2020-234302
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X