Kimura's Disease: A Rare Cause of Unilateral Tonsillar Enlargement.

IF 0.4 Q4 OTORHINOLARYNGOLOGY
Case Reports in Otolaryngology Pub Date : 2021-01-07 eCollection Date: 2021-01-01 DOI:10.1155/2021/8815317
Prakash Khanal, Agya Shrestha
{"title":"Kimura's Disease: A Rare Cause of Unilateral Tonsillar Enlargement.","authors":"Prakash Khanal,&nbsp;Agya Shrestha","doi":"10.1155/2021/8815317","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Kimura's disease is a rare inflammatory disorder of unknown cause, commonly seen in young Asian males. <i>Case Report</i>. A 61-year-old male patient presented with a history of right tonsillar mass and cervical lymphadenopathy. The patient underwent hematological investigation and imaging followed by resection of tonsillar mass. Based on histopathological and subsequent immunohistochemistry reports, the case was diagnosed as Kimura's disease of the tonsil. <i>Discussion</i>. Kimura's disease commonly presents as painless subcutaneous masses in the head and neck region or cervical lymphadenopathy. Kimura's disease presenting as a tonsillar mass is a very rare condition. Patients usually have peripheral eosinophilia and elevated levels of serum IgE. The diagnosis is based on the clinical and histopathologic findings in a biopsy of the mass and/or lymph node along with elevated peripheral eosinophil and serum IgE level.</p><p><strong>Conclusion: </strong>The clinical presentation of Kimura's disease is highly variable. Kimura's disease should be considered as a differential diagnosis in patients presenting with a tonsillar mass. A high index of suspicion along with histopathological examination helps in the early diagnosis and management. Surgical excision is the treatment of choice.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"8815317"},"PeriodicalIF":0.4000,"publicationDate":"2021-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808821/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Otolaryngology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2021/8815317","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Kimura's disease is a rare inflammatory disorder of unknown cause, commonly seen in young Asian males. Case Report. A 61-year-old male patient presented with a history of right tonsillar mass and cervical lymphadenopathy. The patient underwent hematological investigation and imaging followed by resection of tonsillar mass. Based on histopathological and subsequent immunohistochemistry reports, the case was diagnosed as Kimura's disease of the tonsil. Discussion. Kimura's disease commonly presents as painless subcutaneous masses in the head and neck region or cervical lymphadenopathy. Kimura's disease presenting as a tonsillar mass is a very rare condition. Patients usually have peripheral eosinophilia and elevated levels of serum IgE. The diagnosis is based on the clinical and histopathologic findings in a biopsy of the mass and/or lymph node along with elevated peripheral eosinophil and serum IgE level.

Conclusion: The clinical presentation of Kimura's disease is highly variable. Kimura's disease should be considered as a differential diagnosis in patients presenting with a tonsillar mass. A high index of suspicion along with histopathological examination helps in the early diagnosis and management. Surgical excision is the treatment of choice.

Abstract Image

Abstract Image

Abstract Image

木村病:单侧扁桃体肿大的罕见病因。
木村氏病是一种病因不明的罕见炎症性疾病,常见于亚洲年轻男性。病例报告。男性,61岁,以右侧扁桃体肿块及颈淋巴肿大病史为主诉。患者接受血液学检查和影像学检查,并切除扁桃体肿块。根据组织病理学和随后的免疫组织化学报告,该病例被诊断为扁桃体木村病。讨论。木村病通常表现为头颈部无痛皮下肿块或颈部淋巴结病。木村氏病表现为扁桃体肿块是一种非常罕见的疾病。患者通常有外周血嗜酸性粒细胞增多和血清IgE水平升高。诊断是基于肿块和/或淋巴结活检的临床和组织病理学结果,以及外周血嗜酸性粒细胞和血清IgE水平升高。结论:木村病的临床表现多变性。当患者出现扁桃体肿块时,木村氏病应被视为鉴别诊断。高怀疑指数和组织病理学检查有助于早期诊断和治疗。手术切除是治疗的首选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
自引率
0.00%
发文量
20
审稿时长
13 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信