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Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report
RATIONALE: Kimura disease (KD) is a rare, chronic inflammatory disorder characterized by subcutaneous granuloma in the head and neck region, as well as increased eosinophil counts and high serum immunoglobulin E (IgE) levels. Kimura disease is suspected to be an IgE-mediated disease, associated with...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6922356/ https://www.ncbi.nlm.nih.gov/pubmed/31852109 http://dx.doi.org/10.1097/MD.0000000000018300 |
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author | Maehara, Takashi Munemura, Ryusuke Shimizu, Mayumi Kakizoe, Noriko Kaneko, Naoki Murakami, Yuka Masafumi, Moriyama Kiyoshima, Tamotsu Kawano, Shintaro Nakamura, Seiji |
author_facet | Maehara, Takashi Munemura, Ryusuke Shimizu, Mayumi Kakizoe, Noriko Kaneko, Naoki Murakami, Yuka Masafumi, Moriyama Kiyoshima, Tamotsu Kawano, Shintaro Nakamura, Seiji |
author_sort | Maehara, Takashi |
collection | PubMed |
description | RATIONALE: Kimura disease (KD) is a rare, chronic inflammatory disorder characterized by subcutaneous granuloma in the head and neck region, as well as increased eosinophil counts and high serum immunoglobulin E (IgE) levels. Kimura disease is suspected to be an IgE-mediated disease, associated with an allergic response, in which antigen-specific B cells are stimulated to undergo specific IgE class switching with disease-specific CD4+ T (Th) cells help. Thus, exploration of the Th cells in affected tissues with KD is a highly promising field of the investigation. However, there have been no reports with direct evidence to implicate Th cells in affected lesions with KD. Here we quantitatively demonstrate that CD4+ GATA3+ T cells and interleukin (IL)-4+ IgE+ c-kit+ mast cells prominently infiltrate in affected lesion with KD. PATIENT CONCERNS: A 56-year-old Japanese man who exhibited painless swelling in the left parotid region. DIAGNOSES: Diagnosis of KD was made based on characteristic histopathologic findings, in conjunction with peripheral eosinophilia and elevated serum IgE levels. INTERVENTIONS: The patient underwent corticosteroid therapy and had been followed for 2 years. OUTCOMES: We report a rare case of KD of the parotid region in a 56-year-old man, followed by corticosteroid therapy for 2 years. The mass decreased in size and skin itchiness decreased after therapy. He was discharged without any complications. Furthermore, we quantitatively demonstrate the dominance of CD4+ GATA3+ T cells in affected tissues of KD and detect IL-4+ IgE+ c-kit+ mast cells in lesions by multicolor staining approaches. LESSONS: The findings from this case suggest that peripheral blood eosinophilia might serve as a marker of recurrent disease, long-term follow-up is necessary due to the possibility of recurrent. Interactions among expanded IgE+ B cells, CD4+ GATA3+ T cells, eosinophils, and activated mast cells might play a critical role in the pathogenesis of KD. |
format | Online Article Text |
id | pubmed-6922356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-69223562020-01-23 Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report Maehara, Takashi Munemura, Ryusuke Shimizu, Mayumi Kakizoe, Noriko Kaneko, Naoki Murakami, Yuka Masafumi, Moriyama Kiyoshima, Tamotsu Kawano, Shintaro Nakamura, Seiji Medicine (Baltimore) 3600 RATIONALE: Kimura disease (KD) is a rare, chronic inflammatory disorder characterized by subcutaneous granuloma in the head and neck region, as well as increased eosinophil counts and high serum immunoglobulin E (IgE) levels. Kimura disease is suspected to be an IgE-mediated disease, associated with an allergic response, in which antigen-specific B cells are stimulated to undergo specific IgE class switching with disease-specific CD4+ T (Th) cells help. Thus, exploration of the Th cells in affected tissues with KD is a highly promising field of the investigation. However, there have been no reports with direct evidence to implicate Th cells in affected lesions with KD. Here we quantitatively demonstrate that CD4+ GATA3+ T cells and interleukin (IL)-4+ IgE+ c-kit+ mast cells prominently infiltrate in affected lesion with KD. PATIENT CONCERNS: A 56-year-old Japanese man who exhibited painless swelling in the left parotid region. DIAGNOSES: Diagnosis of KD was made based on characteristic histopathologic findings, in conjunction with peripheral eosinophilia and elevated serum IgE levels. INTERVENTIONS: The patient underwent corticosteroid therapy and had been followed for 2 years. OUTCOMES: We report a rare case of KD of the parotid region in a 56-year-old man, followed by corticosteroid therapy for 2 years. The mass decreased in size and skin itchiness decreased after therapy. He was discharged without any complications. Furthermore, we quantitatively demonstrate the dominance of CD4+ GATA3+ T cells in affected tissues of KD and detect IL-4+ IgE+ c-kit+ mast cells in lesions by multicolor staining approaches. LESSONS: The findings from this case suggest that peripheral blood eosinophilia might serve as a marker of recurrent disease, long-term follow-up is necessary due to the possibility of recurrent. Interactions among expanded IgE+ B cells, CD4+ GATA3+ T cells, eosinophils, and activated mast cells might play a critical role in the pathogenesis of KD. Wolters Kluwer Health 2019-12-16 /pmc/articles/PMC6922356/ /pubmed/31852109 http://dx.doi.org/10.1097/MD.0000000000018300 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 3600 Maehara, Takashi Munemura, Ryusuke Shimizu, Mayumi Kakizoe, Noriko Kaneko, Naoki Murakami, Yuka Masafumi, Moriyama Kiyoshima, Tamotsu Kawano, Shintaro Nakamura, Seiji Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report |
title | Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report |
title_full | Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report |
title_fullStr | Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report |
title_full_unstemmed | Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report |
title_short | Tissue-infiltrating immune cells contribute to understanding the pathogenesis of Kimura disease: A case report |
title_sort | tissue-infiltrating immune cells contribute to understanding the pathogenesis of kimura disease: a case report |
topic | 3600 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6922356/ https://www.ncbi.nlm.nih.gov/pubmed/31852109 http://dx.doi.org/10.1097/MD.0000000000018300 |
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