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A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels

BACKGROUND: The clinical features and laboratory parameters of patients with Kawasaki disease (KD) and systemic juvenile idiopathic arthritis (sJIA) occasionally overlap. Therefore, serum levels of cytokine and ferritin are used as markers to distinguish between KD and sJIA. KD patients have a high...

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Autores principales: Noto, Takanori, Seto, Hiroki, Fukuhara, Junji, Murabayashi, Masao, Yachie, Akihiro, Ayusawa, Mamoru, Morioka, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291954/
https://www.ncbi.nlm.nih.gov/pubmed/30541507
http://dx.doi.org/10.1186/s12887-018-1365-7
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author Noto, Takanori
Seto, Hiroki
Fukuhara, Junji
Murabayashi, Masao
Yachie, Akihiro
Ayusawa, Mamoru
Morioka, Ichiro
author_facet Noto, Takanori
Seto, Hiroki
Fukuhara, Junji
Murabayashi, Masao
Yachie, Akihiro
Ayusawa, Mamoru
Morioka, Ichiro
author_sort Noto, Takanori
collection PubMed
description BACKGROUND: The clinical features and laboratory parameters of patients with Kawasaki disease (KD) and systemic juvenile idiopathic arthritis (sJIA) occasionally overlap. Therefore, serum levels of cytokine and ferritin are used as markers to distinguish between KD and sJIA. KD patients have a high level of interleukin (IL)-6, low level of IL-18, and no elevation of the level of serum ferritin. Conversely, sJIA patients have a low level of IL-6 and high levels of IL-18 and ferritin in the serum. However, to the best of our knowledge, no case report of KD with a low serum level of IL-6 and extremely high levels of IL-18 and ferritin is found. CASE PRESENTATION: A 6-year-old boy presented with a history of fever for 9 days and a rash that appeared 7 days from the onset. He was diagnosed with incomplete KD because of fever, skin rash, oral cavity erythematous changes, and erythema and edema of the hands with laboratory findings of serum albumin level < 3.0 g/dL, elevated alanine aminotransferase level and leukocyturia. Intravenous immunoglobulin and prednisolone and oral aspirin were introduced on the 10th day. Fever subsided 1 day after initiating the treatment, but arthritis of both knees appeared in addition to hepatosplenomegaly. We suspected sJIA, as the serum level of ferritin was 19,740 ng/mL, IL-6 was < 3 pg/mL, and IL-18 was 132,000 pg/mL. Skin desquamation of the fingertips was observed 18 days from the onset; thus, he was finally diagnosed with incomplete KD with arthritis. At 32 days from the onset, we stopped the prednisolone therapy and no symptoms of relapse were observed afterwards. In the follow-up at 16 months from the onset, he had neither signs of active joint or skin involvement, nor cardiac involvement. CONCLUSIONS: Although patients with sJIA generally have high serum levels of IL-18 and ferritin, this was a case of incomplete KD with extremely high serum levels of IL-18 and ferritin. Serum cytokine and ferritin are often used for the differential diagnosis of KD and sJIA. We need to recognize the existence of KD with high serum levels of IL-18 and ferritin.
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spelling pubmed-62919542018-12-17 A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels Noto, Takanori Seto, Hiroki Fukuhara, Junji Murabayashi, Masao Yachie, Akihiro Ayusawa, Mamoru Morioka, Ichiro BMC Pediatr Case Report BACKGROUND: The clinical features and laboratory parameters of patients with Kawasaki disease (KD) and systemic juvenile idiopathic arthritis (sJIA) occasionally overlap. Therefore, serum levels of cytokine and ferritin are used as markers to distinguish between KD and sJIA. KD patients have a high level of interleukin (IL)-6, low level of IL-18, and no elevation of the level of serum ferritin. Conversely, sJIA patients have a low level of IL-6 and high levels of IL-18 and ferritin in the serum. However, to the best of our knowledge, no case report of KD with a low serum level of IL-6 and extremely high levels of IL-18 and ferritin is found. CASE PRESENTATION: A 6-year-old boy presented with a history of fever for 9 days and a rash that appeared 7 days from the onset. He was diagnosed with incomplete KD because of fever, skin rash, oral cavity erythematous changes, and erythema and edema of the hands with laboratory findings of serum albumin level < 3.0 g/dL, elevated alanine aminotransferase level and leukocyturia. Intravenous immunoglobulin and prednisolone and oral aspirin were introduced on the 10th day. Fever subsided 1 day after initiating the treatment, but arthritis of both knees appeared in addition to hepatosplenomegaly. We suspected sJIA, as the serum level of ferritin was 19,740 ng/mL, IL-6 was < 3 pg/mL, and IL-18 was 132,000 pg/mL. Skin desquamation of the fingertips was observed 18 days from the onset; thus, he was finally diagnosed with incomplete KD with arthritis. At 32 days from the onset, we stopped the prednisolone therapy and no symptoms of relapse were observed afterwards. In the follow-up at 16 months from the onset, he had neither signs of active joint or skin involvement, nor cardiac involvement. CONCLUSIONS: Although patients with sJIA generally have high serum levels of IL-18 and ferritin, this was a case of incomplete KD with extremely high serum levels of IL-18 and ferritin. Serum cytokine and ferritin are often used for the differential diagnosis of KD and sJIA. We need to recognize the existence of KD with high serum levels of IL-18 and ferritin. BioMed Central 2018-12-12 /pmc/articles/PMC6291954/ /pubmed/30541507 http://dx.doi.org/10.1186/s12887-018-1365-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Noto, Takanori
Seto, Hiroki
Fukuhara, Junji
Murabayashi, Masao
Yachie, Akihiro
Ayusawa, Mamoru
Morioka, Ichiro
A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels
title A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels
title_full A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels
title_fullStr A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels
title_full_unstemmed A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels
title_short A case of incomplete Kawasaki disease with extremely high serum ferritin and interleukin-18 levels
title_sort case of incomplete kawasaki disease with extremely high serum ferritin and interleukin-18 levels
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291954/
https://www.ncbi.nlm.nih.gov/pubmed/30541507
http://dx.doi.org/10.1186/s12887-018-1365-7
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