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The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report
BACKGROUND: Kikuchi–Fujimoto disease is an uncommon systemic disease that mostly affects young women. Kikuchi–Fujimoto disease typically manifests as necrotizing lymphadenopathy, which frequently follows by a fever; however, Kikuchi–Fujimoto disease occurs rarely in extranodal regions. One of the mo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605312/ https://www.ncbi.nlm.nih.gov/pubmed/37884991 http://dx.doi.org/10.1186/s13256-023-04186-4 |
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author | Yousefi, Maysam Rukerd, Mohammad Rezaei Zadeh Binafar, Hanieh Shoaie, Sahar Mirkamali, Hanieh Pourzand, Pouria Kaveh, Roxana |
author_facet | Yousefi, Maysam Rukerd, Mohammad Rezaei Zadeh Binafar, Hanieh Shoaie, Sahar Mirkamali, Hanieh Pourzand, Pouria Kaveh, Roxana |
author_sort | Yousefi, Maysam |
collection | PubMed |
description | BACKGROUND: Kikuchi–Fujimoto disease is an uncommon systemic disease that mostly affects young women. Kikuchi–Fujimoto disease typically manifests as necrotizing lymphadenopathy, which frequently follows by a fever; however, Kikuchi–Fujimoto disease occurs rarely in extranodal regions. One of the most important accompaniments of Kikuchi–Fujimoto disease is its connection with autoimmune diseases such as systemic lupus erythematosus. This case presents a simultaneous occurrence of Kikuchi–Fujimoto disease with liver involvement and systemic lupus erythematosus in a young female patient. CASE PRESENTATION: We present a rare case of a 20-year-old white woman who presented with fever, joint pains, myalgia, and shortness of breath. Initial hospitalization and treatment for fever of unknown origin did not yield improvement. Physical examination revealed cervical and supraclavicular lymphadenopathy, and laboratory investigations showed abnormal blood counts, elevated inflammatory markers, and positive autoimmune serologies. Imaging studies revealed bilateral pleural effusion and liver lesions. Lymph node biopsy confirmed the diagnosis of Kikuchi–Fujimoto disease, and liver biopsy showed extranodal involvement. The patient was diagnosed with Kikuchi–Fujimoto disease-associated systemic lupus erythematosus and treated with hydroxychloroquine and corticosteroids. The patient showed gradual resolution of symptoms and lymphadenopathy with treatment. CONCLUSION: Kikuchi–Fujimoto disease is a rare systemic condition primarily impacting young females. It is characterized by necrotizing lymphadenopathy, often accompanied by fever. Although Kikuchi–Fujimoto disease is predominantly seen in the lymph nodes, occurrences in non-nodal areas are infrequent. When diagnosing Kikuchi–Fujimoto disease, it is essential to screen patients for systemic lupus erythematosus. In this particular case, we observed liver involvement along with the presence of both Kikuchi–Fujimoto disease and systemic lupus erythematosus. |
format | Online Article Text |
id | pubmed-10605312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106053122023-10-28 The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report Yousefi, Maysam Rukerd, Mohammad Rezaei Zadeh Binafar, Hanieh Shoaie, Sahar Mirkamali, Hanieh Pourzand, Pouria Kaveh, Roxana J Med Case Rep Case Report BACKGROUND: Kikuchi–Fujimoto disease is an uncommon systemic disease that mostly affects young women. Kikuchi–Fujimoto disease typically manifests as necrotizing lymphadenopathy, which frequently follows by a fever; however, Kikuchi–Fujimoto disease occurs rarely in extranodal regions. One of the most important accompaniments of Kikuchi–Fujimoto disease is its connection with autoimmune diseases such as systemic lupus erythematosus. This case presents a simultaneous occurrence of Kikuchi–Fujimoto disease with liver involvement and systemic lupus erythematosus in a young female patient. CASE PRESENTATION: We present a rare case of a 20-year-old white woman who presented with fever, joint pains, myalgia, and shortness of breath. Initial hospitalization and treatment for fever of unknown origin did not yield improvement. Physical examination revealed cervical and supraclavicular lymphadenopathy, and laboratory investigations showed abnormal blood counts, elevated inflammatory markers, and positive autoimmune serologies. Imaging studies revealed bilateral pleural effusion and liver lesions. Lymph node biopsy confirmed the diagnosis of Kikuchi–Fujimoto disease, and liver biopsy showed extranodal involvement. The patient was diagnosed with Kikuchi–Fujimoto disease-associated systemic lupus erythematosus and treated with hydroxychloroquine and corticosteroids. The patient showed gradual resolution of symptoms and lymphadenopathy with treatment. CONCLUSION: Kikuchi–Fujimoto disease is a rare systemic condition primarily impacting young females. It is characterized by necrotizing lymphadenopathy, often accompanied by fever. Although Kikuchi–Fujimoto disease is predominantly seen in the lymph nodes, occurrences in non-nodal areas are infrequent. When diagnosing Kikuchi–Fujimoto disease, it is essential to screen patients for systemic lupus erythematosus. In this particular case, we observed liver involvement along with the presence of both Kikuchi–Fujimoto disease and systemic lupus erythematosus. BioMed Central 2023-10-27 /pmc/articles/PMC10605312/ /pubmed/37884991 http://dx.doi.org/10.1186/s13256-023-04186-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Yousefi, Maysam Rukerd, Mohammad Rezaei Zadeh Binafar, Hanieh Shoaie, Sahar Mirkamali, Hanieh Pourzand, Pouria Kaveh, Roxana The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report |
title | The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report |
title_full | The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report |
title_fullStr | The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report |
title_full_unstemmed | The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report |
title_short | The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report |
title_sort | co-occurrence of kikuchi–fujimoto disease and systemic lupus erythematosus: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605312/ https://www.ncbi.nlm.nih.gov/pubmed/37884991 http://dx.doi.org/10.1186/s13256-023-04186-4 |
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