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Kimura's disease successively affecting multiple body parts: a case-based literature review

BACKGROUND: Kimura’s disease is a rare, benign, chronic inflammatory disease that presents as painless, solid masses mainly affecting the deep subcutaneous areas of the head and neck, especially the salivary glands, parotid glands and nearby lymph nodes. It is characterized by elevated peripheral bl...

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Autores principales: Yang, Baodi, Liao, Hailan, Wang, Minghua, Long, Qiaoyan, Zhong, Huanhuan, Luo, Lin, Liu, Zhongmin, Cheng, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977031/
https://www.ncbi.nlm.nih.gov/pubmed/35366827
http://dx.doi.org/10.1186/s12886-022-02378-y
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author Yang, Baodi
Liao, Hailan
Wang, Minghua
Long, Qiaoyan
Zhong, Huanhuan
Luo, Lin
Liu, Zhongmin
Cheng, Xiaohui
author_facet Yang, Baodi
Liao, Hailan
Wang, Minghua
Long, Qiaoyan
Zhong, Huanhuan
Luo, Lin
Liu, Zhongmin
Cheng, Xiaohui
author_sort Yang, Baodi
collection PubMed
description BACKGROUND: Kimura’s disease is a rare, benign, chronic inflammatory disease that presents as painless, solid masses mainly affecting the deep subcutaneous areas of the head and neck, especially the salivary glands, parotid glands and nearby lymph nodes. It is characterized by elevated peripheral blood eosinophil and Immunoglobulin E (IgE) levels. CASE PRESENTATION: A 31-year-old Asian male presented with an orbital space-occupying lesion lasting for 1.5 years. Ten years prior, surgical excision of bilateral fossa cubitalis and groin masses was performed, and the pathological examination showed "lymphoproliferative disease". One year later, masses reappeared near the surgical sites; they grew slowly and shrank after glucocorticoid treatment. At this point, admission examinations showed in the peripheral blood an eosinophil proportion of 13.4%, a total IgE level of 26,900.00 IU/mL, prurigo present on the whole body, and multiple palpable masses near the bilateral fossa cubitalis and groin. The left eyeball was exophthalmic. The left elbow mass was excised, and the pathological examination confirmed Kimura’s disease. Oral glucocorticoid therapy is taken and tapering regularly. The eosinophil count returned to normal, the IgE level gradually decreased, the orbital space-occupying lesion and elbow and groin masses shrank significantly, and the whole-body skin prurigo disappeared. Currently, the patient has been in a stable condition for eighteen months. CONCLUSION: Our case provides a novel insight that Kimura’s disease should be involved in the differential diagnosis of inflammatory lesion mass of orbit and also supports systemic regular glucocorticoid as a valuable therapy of such condition, but close follow-up and long-term observation are crucial.
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spelling pubmed-89770312022-04-04 Kimura's disease successively affecting multiple body parts: a case-based literature review Yang, Baodi Liao, Hailan Wang, Minghua Long, Qiaoyan Zhong, Huanhuan Luo, Lin Liu, Zhongmin Cheng, Xiaohui BMC Ophthalmol Case Report BACKGROUND: Kimura’s disease is a rare, benign, chronic inflammatory disease that presents as painless, solid masses mainly affecting the deep subcutaneous areas of the head and neck, especially the salivary glands, parotid glands and nearby lymph nodes. It is characterized by elevated peripheral blood eosinophil and Immunoglobulin E (IgE) levels. CASE PRESENTATION: A 31-year-old Asian male presented with an orbital space-occupying lesion lasting for 1.5 years. Ten years prior, surgical excision of bilateral fossa cubitalis and groin masses was performed, and the pathological examination showed "lymphoproliferative disease". One year later, masses reappeared near the surgical sites; they grew slowly and shrank after glucocorticoid treatment. At this point, admission examinations showed in the peripheral blood an eosinophil proportion of 13.4%, a total IgE level of 26,900.00 IU/mL, prurigo present on the whole body, and multiple palpable masses near the bilateral fossa cubitalis and groin. The left eyeball was exophthalmic. The left elbow mass was excised, and the pathological examination confirmed Kimura’s disease. Oral glucocorticoid therapy is taken and tapering regularly. The eosinophil count returned to normal, the IgE level gradually decreased, the orbital space-occupying lesion and elbow and groin masses shrank significantly, and the whole-body skin prurigo disappeared. Currently, the patient has been in a stable condition for eighteen months. CONCLUSION: Our case provides a novel insight that Kimura’s disease should be involved in the differential diagnosis of inflammatory lesion mass of orbit and also supports systemic regular glucocorticoid as a valuable therapy of such condition, but close follow-up and long-term observation are crucial. BioMed Central 2022-04-02 /pmc/articles/PMC8977031/ /pubmed/35366827 http://dx.doi.org/10.1186/s12886-022-02378-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Yang, Baodi
Liao, Hailan
Wang, Minghua
Long, Qiaoyan
Zhong, Huanhuan
Luo, Lin
Liu, Zhongmin
Cheng, Xiaohui
Kimura's disease successively affecting multiple body parts: a case-based literature review
title Kimura's disease successively affecting multiple body parts: a case-based literature review
title_full Kimura's disease successively affecting multiple body parts: a case-based literature review
title_fullStr Kimura's disease successively affecting multiple body parts: a case-based literature review
title_full_unstemmed Kimura's disease successively affecting multiple body parts: a case-based literature review
title_short Kimura's disease successively affecting multiple body parts: a case-based literature review
title_sort kimura's disease successively affecting multiple body parts: a case-based literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977031/
https://www.ncbi.nlm.nih.gov/pubmed/35366827
http://dx.doi.org/10.1186/s12886-022-02378-y
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