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Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease

Kikuchi-Fujimoto disease (KFD) is a rare, benign disorder that typically follows a self-limiting natural course and was initially described in young females of Asian descent. Its clinical presentation may mimic lymphoproliferative disorders, connective tissue disorders, and chronic infections. This...

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Autores principales: Vu, Duy, Reddy, Srini, Day, Lynn, Aydin, Nail, Misra, Subhasis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844816/
https://www.ncbi.nlm.nih.gov/pubmed/27162600
http://dx.doi.org/10.4081/cp.2016.828
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author Vu, Duy
Reddy, Srini
Day, Lynn
Aydin, Nail
Misra, Subhasis
author_facet Vu, Duy
Reddy, Srini
Day, Lynn
Aydin, Nail
Misra, Subhasis
author_sort Vu, Duy
collection PubMed
description Kikuchi-Fujimoto disease (KFD) is a rare, benign disorder that typically follows a self-limiting natural course and was initially described in young females of Asian descent. Its clinical presentation may mimic lymphoproliferative disorders, connective tissue disorders, and chronic infections. This often leads to misdiagnosis and inappropriate treatment. The exact cause of this condition remains unknown although autoimmune processes and certain infectious agents have been associated with the disease. The diagnosis of KFD is made histopathologically. Treatment is supportive and long-term follow-up is recommended due to increased risk of future development of systemic lupus erythematosus. Here we are presenting a case of a patient with an unusual presentation of KFD.
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spelling pubmed-48448162016-05-09 Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease Vu, Duy Reddy, Srini Day, Lynn Aydin, Nail Misra, Subhasis Clin Pract Case Report Kikuchi-Fujimoto disease (KFD) is a rare, benign disorder that typically follows a self-limiting natural course and was initially described in young females of Asian descent. Its clinical presentation may mimic lymphoproliferative disorders, connective tissue disorders, and chronic infections. This often leads to misdiagnosis and inappropriate treatment. The exact cause of this condition remains unknown although autoimmune processes and certain infectious agents have been associated with the disease. The diagnosis of KFD is made histopathologically. Treatment is supportive and long-term follow-up is recommended due to increased risk of future development of systemic lupus erythematosus. Here we are presenting a case of a patient with an unusual presentation of KFD. PAGEPress Publications, Pavia, Italy 2015-04-19 /pmc/articles/PMC4844816/ /pubmed/27162600 http://dx.doi.org/10.4081/cp.2016.828 Text en ©Copyright D. Vu et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Vu, Duy
Reddy, Srini
Day, Lynn
Aydin, Nail
Misra, Subhasis
Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease
title Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease
title_full Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease
title_fullStr Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease
title_full_unstemmed Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease
title_short Kikuchi-Fujimoto Disease: Unusual Presentation of Rare Disease
title_sort kikuchi-fujimoto disease: unusual presentation of rare disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844816/
https://www.ncbi.nlm.nih.gov/pubmed/27162600
http://dx.doi.org/10.4081/cp.2016.828
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