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Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy

Introduction. Kimura's disease is a rare chronic inflammatory disorder characterized by the head and neck lymphadenopathy often accompanied by eosinophilia and elevated serum IgE. It is benign condition with unknown etiology usually affecting young men of Asian race. Affected Caucasians are ver...

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Autores principales: Osuch-Wójcikiewicz, Ewa, Bruzgielewicz, Antoni, Lachowska, Magdalena, Wasilewska, Agata, Niemczyk, Kazimierz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052045/
https://www.ncbi.nlm.nih.gov/pubmed/24955268
http://dx.doi.org/10.1155/2014/415865
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author Osuch-Wójcikiewicz, Ewa
Bruzgielewicz, Antoni
Lachowska, Magdalena
Wasilewska, Agata
Niemczyk, Kazimierz
author_facet Osuch-Wójcikiewicz, Ewa
Bruzgielewicz, Antoni
Lachowska, Magdalena
Wasilewska, Agata
Niemczyk, Kazimierz
author_sort Osuch-Wójcikiewicz, Ewa
collection PubMed
description Introduction. Kimura's disease is a rare chronic inflammatory disorder characterized by the head and neck lymphadenopathy often accompanied by eosinophilia and elevated serum IgE. It is benign condition with unknown etiology usually affecting young men of Asian race. Affected Caucasians are very rare. Case Presentation. We report a clinically and histopathologically typical case of this disease in a 40-year-old Caucasian female. In differential diagnosis particular attention has been paid to angiolymphoid hyperplasia with eosinophilia and neoplasms. Conclusion. The diagnosis of Kimura's disease can be very difficult and misleading; it is important not to ignore histopathological features. The presented patient has been under follow-up with no more symptoms of the disease for the last 1.5 years.
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spelling pubmed-40520452014-06-22 Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy Osuch-Wójcikiewicz, Ewa Bruzgielewicz, Antoni Lachowska, Magdalena Wasilewska, Agata Niemczyk, Kazimierz Case Rep Otolaryngol Case Report Introduction. Kimura's disease is a rare chronic inflammatory disorder characterized by the head and neck lymphadenopathy often accompanied by eosinophilia and elevated serum IgE. It is benign condition with unknown etiology usually affecting young men of Asian race. Affected Caucasians are very rare. Case Presentation. We report a clinically and histopathologically typical case of this disease in a 40-year-old Caucasian female. In differential diagnosis particular attention has been paid to angiolymphoid hyperplasia with eosinophilia and neoplasms. Conclusion. The diagnosis of Kimura's disease can be very difficult and misleading; it is important not to ignore histopathological features. The presented patient has been under follow-up with no more symptoms of the disease for the last 1.5 years. Hindawi Publishing Corporation 2014 2014-05-14 /pmc/articles/PMC4052045/ /pubmed/24955268 http://dx.doi.org/10.1155/2014/415865 Text en Copyright © 2014 Ewa Osuch-Wójcikiewicz et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Osuch-Wójcikiewicz, Ewa
Bruzgielewicz, Antoni
Lachowska, Magdalena
Wasilewska, Agata
Niemczyk, Kazimierz
Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy
title Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy
title_full Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy
title_fullStr Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy
title_full_unstemmed Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy
title_short Kimura's Disease in a Caucasian Female: A Very Rare Cause of Lymphadenopathy
title_sort kimura's disease in a caucasian female: a very rare cause of lymphadenopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052045/
https://www.ncbi.nlm.nih.gov/pubmed/24955268
http://dx.doi.org/10.1155/2014/415865
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