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Kikuchi Fujimoto disease: sinister presentation, good prognosis

Kikuchi-Fujimoto disease (KFD) is a rare, benign, self-limiting necrotizing lymphadenitis of unknown etiology. The disease can affect people of all ages and of any sex and ethnicity. Tissue biopsy is needed for accurate diagnosis. The condition commonly masquerades as more sinister conditions such a...

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Autores principales: Jiwani, Rahim A., Jourdan, Daniel N., Pona, Adrian, Donthi, Deepak, Stalls, J. Stephen, Rehana, Rita W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7850461/
https://www.ncbi.nlm.nih.gov/pubmed/33552420
http://dx.doi.org/10.1080/20009666.2020.1824332
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author Jiwani, Rahim A.
Jourdan, Daniel N.
Pona, Adrian
Donthi, Deepak
Stalls, J. Stephen
Rehana, Rita W.
author_facet Jiwani, Rahim A.
Jourdan, Daniel N.
Pona, Adrian
Donthi, Deepak
Stalls, J. Stephen
Rehana, Rita W.
author_sort Jiwani, Rahim A.
collection PubMed
description Kikuchi-Fujimoto disease (KFD) is a rare, benign, self-limiting necrotizing lymphadenitis of unknown etiology. The disease can affect people of all ages and of any sex and ethnicity. Tissue biopsy is needed for accurate diagnosis. The condition commonly masquerades as more sinister conditions such as malignancy and rheumatologic disorders, but has a much better prognosis. Treatment is generally supportive but patients may require corticosteroids with eventual spontaneous resolution. We discuss a case of KFD in a 34-year-old male and highlight the need for prompt and accurate diagnosis.
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spelling pubmed-78504612021-02-05 Kikuchi Fujimoto disease: sinister presentation, good prognosis Jiwani, Rahim A. Jourdan, Daniel N. Pona, Adrian Donthi, Deepak Stalls, J. Stephen Rehana, Rita W. J Community Hosp Intern Med Perspect Case Report Kikuchi-Fujimoto disease (KFD) is a rare, benign, self-limiting necrotizing lymphadenitis of unknown etiology. The disease can affect people of all ages and of any sex and ethnicity. Tissue biopsy is needed for accurate diagnosis. The condition commonly masquerades as more sinister conditions such as malignancy and rheumatologic disorders, but has a much better prognosis. Treatment is generally supportive but patients may require corticosteroids with eventual spontaneous resolution. We discuss a case of KFD in a 34-year-old male and highlight the need for prompt and accurate diagnosis. Taylor & Francis 2021-01-26 /pmc/articles/PMC7850461/ /pubmed/33552420 http://dx.doi.org/10.1080/20009666.2020.1824332 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jiwani, Rahim A.
Jourdan, Daniel N.
Pona, Adrian
Donthi, Deepak
Stalls, J. Stephen
Rehana, Rita W.
Kikuchi Fujimoto disease: sinister presentation, good prognosis
title Kikuchi Fujimoto disease: sinister presentation, good prognosis
title_full Kikuchi Fujimoto disease: sinister presentation, good prognosis
title_fullStr Kikuchi Fujimoto disease: sinister presentation, good prognosis
title_full_unstemmed Kikuchi Fujimoto disease: sinister presentation, good prognosis
title_short Kikuchi Fujimoto disease: sinister presentation, good prognosis
title_sort kikuchi fujimoto disease: sinister presentation, good prognosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7850461/
https://www.ncbi.nlm.nih.gov/pubmed/33552420
http://dx.doi.org/10.1080/20009666.2020.1824332
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