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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2015
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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. |
format | Online Article Text |
id | pubmed-4844816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
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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