首页> 外文期刊>journal of indian academy of oral medicine and radiology >Kimura Disease: A Rare Case with Multiple Recurrences involving Subcutaneous Tissue, Parotid Gland, and Lymph Nodes
【24h】

Kimura Disease: A Rare Case with Multiple Recurrences involving Subcutaneous Tissue, Parotid Gland, and Lymph Nodes

机译:木村病:一种罕见的病例,累及皮下组织、腮腺和淋巴结的多次复发

获取原文

摘要

© 2024 Journal of Indian Academy of Oral Medicine Radiology.Kimura disease (KD) is an uncommon, long-standing inflammatory condition affecting the head and neck that has no recognized cause. It typically appears as a painless subcutaneous nodule mimicking a tumor. The characteristic triad other the painless subcutaneous masses include elevated serum immunoglobulin E and peripheral eosinophilia. We present a unique instance of KD involving a male individual, age 23 years, who has swelling in the pre-auricular area on the left side of the face. Establishing KD as a probable differential diagnosis is the key to prompt treatment, declining misdiagnosis, and enhancing the quality of the patient's life.
机译:© 2024 Journal of Indian Academy of Oral Medicine & Radiology.木村病 (KD) 是一种罕见的、长期影响头部和颈部的炎症性疾病,原因不明。它通常表现为模仿肿瘤的无痛皮下结节。除无痛性皮下肿块外,特征性三联征包括血清免疫球蛋白 E 升高和外周嗜酸性粒细胞增多。我们介绍了一个独特的川崎病实例,涉及一名 23 岁的男性个体,他在面部左侧耳前区域肿胀。将川崎病确定为可能的鉴别诊断是及时治疗、减少误诊和提高患者生活质量的关键。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号