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Kikuchi–Fujimoto disease and systemic lupus erythematosus
Kikuchi–Fujimoto disease, or histiocytic necrotizing lymphadenitis, is an infrequent idiopathic disorder. It has been associated with autoimmune disorders, of which systemic lupus erythematosus is the most outstanding. The basis of its diagnosis relies on the histological examination of lymph nodes,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935008/ https://www.ncbi.nlm.nih.gov/pubmed/27418858 http://dx.doi.org/10.2147/IMCRJ.S106396 |
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author | Baenas, Diego F Diehl, Fernando A Haye Salinas, María J Riva, Verónica Diller, Ana Lemos, Pablo A |
author_facet | Baenas, Diego F Diehl, Fernando A Haye Salinas, María J Riva, Verónica Diller, Ana Lemos, Pablo A |
author_sort | Baenas, Diego F |
collection | PubMed |
description | Kikuchi–Fujimoto disease, or histiocytic necrotizing lymphadenitis, is an infrequent idiopathic disorder. It has been associated with autoimmune disorders, of which systemic lupus erythematosus is the most outstanding. The basis of its diagnosis relies on the histological examination of lymph nodes, which typically reveals necrosis surrounded by histiocytes with crescentic nucleus, immunoblasts and plasma cells, and absence of neutrophils. We report the case of a 27-year-old Argentinian female patient without any relevant past medical history to demonstrate the correlation between Kikuchi–Fujimoto disease and systemic lupus erythematosus. |
format | Online Article Text |
id | pubmed-4935008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49350082016-07-14 Kikuchi–Fujimoto disease and systemic lupus erythematosus Baenas, Diego F Diehl, Fernando A Haye Salinas, María J Riva, Verónica Diller, Ana Lemos, Pablo A Int Med Case Rep J Case-Report Kikuchi–Fujimoto disease, or histiocytic necrotizing lymphadenitis, is an infrequent idiopathic disorder. It has been associated with autoimmune disorders, of which systemic lupus erythematosus is the most outstanding. The basis of its diagnosis relies on the histological examination of lymph nodes, which typically reveals necrosis surrounded by histiocytes with crescentic nucleus, immunoblasts and plasma cells, and absence of neutrophils. We report the case of a 27-year-old Argentinian female patient without any relevant past medical history to demonstrate the correlation between Kikuchi–Fujimoto disease and systemic lupus erythematosus. Dove Medical Press 2016-06-29 /pmc/articles/PMC4935008/ /pubmed/27418858 http://dx.doi.org/10.2147/IMCRJ.S106396 Text en © 2016 Baenas et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case-Report Baenas, Diego F Diehl, Fernando A Haye Salinas, María J Riva, Verónica Diller, Ana Lemos, Pablo A Kikuchi–Fujimoto disease and systemic lupus erythematosus |
title | Kikuchi–Fujimoto disease and systemic lupus erythematosus |
title_full | Kikuchi–Fujimoto disease and systemic lupus erythematosus |
title_fullStr | Kikuchi–Fujimoto disease and systemic lupus erythematosus |
title_full_unstemmed | Kikuchi–Fujimoto disease and systemic lupus erythematosus |
title_short | Kikuchi–Fujimoto disease and systemic lupus erythematosus |
title_sort | kikuchi–fujimoto disease and systemic lupus erythematosus |
topic | Case-Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935008/ https://www.ncbi.nlm.nih.gov/pubmed/27418858 http://dx.doi.org/10.2147/IMCRJ.S106396 |
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