Clinical heterogeneity and prognostic markers in head and neck Kimura disease: A retrospective study.

IF 2.2
Yifan Yang, Xue Zhang, Qi Zhong, Yang Zhang, Hongzhi Ma, Lizhen Hou, Shizhi He, Qian Shi, Ru Wang, Jugao Fang, Ling Feng
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Abstract

Objective: Kimura disease (KD) is a rare, chronic inflammatory disorder that is typically located in the head and neck region. It is characterized by subcutaneous nodules, eosinophilia, and elevated IgE levels. Its unclear etiology and similarities to malignancies create diagnostic and therapeutic challenges. The purpose of this study is to share our treatment experience and explore prognostic factors associated with KD.

Methods: We collected data on KD patients treated at our hospital between June 2013 and May 2024. The data included the patients' demographics, clinical and laboratory profiles, radiological and pathological findings, treatments, and outcomes. Non-normal variables are presented as medians with ranges, and categorical variables are shown as frequencies. We performed statistical comparisons using Mann-Whitney U tests.

Results: This study analyzed 13 KD patients (median age 44 years, male-to-female ratio 9:4). All patients present with had head and neck lesions. 75.0% showed elevated peripheral eosinophilia, 77.8% had increased blood eosinophilia percentages, and all tested patients had elevated IgE levels. Treatments included surgical excision, glucocorticoids, methotrexate, low-dose radiotherapy, and observation. Remission was achieved in 76.9% of patients. Patients with poor outcomes had significantly higher absolute eosinophil counts (median: 1.77 vs. 0.90 × 10⁹/L, p = 0.04) and percentages (median: 21.4% vs. 12.2%, p = 0.03) than those with favorable outcomes. Imaging misdiagnosis occurred in 38.5% of patients, highlighting the superiority of histopathology for diagnosis. Urine abnormalities, mild renal dysfunction, and uncommon lesion sites were also observed.

Conclusion: The clinical heterogeneity of KD requires multidisciplinary management. Pre-treatment eosinophilia is emerging as a prognostic marker. Future studies should prioritize the identification of biomarkers, kinetic surveillance, and targeted biologics in order to reduce recurrence and systemic complications.

头颈部木村病的临床异质性和预后指标:一项回顾性研究
目的:木村病(KD)是一种罕见的慢性炎症性疾病,通常位于头颈部。其特征是皮下结节、嗜酸性粒细胞增多和IgE水平升高。其病因不明和与恶性肿瘤的相似性给诊断和治疗带来了挑战。本研究的目的是分享我们的治疗经验,并探讨与KD相关的预后因素。方法:收集2013年6月至2024年5月在我院治疗的KD患者的数据。这些数据包括患者的人口统计资料、临床和实验室资料、放射学和病理学结果、治疗和结果。非正态变量表示为带范围的中位数,分类变量表示为频率。我们使用Mann-Whitney U检验进行统计比较。结果:本研究分析了13例KD患者(中位年龄44岁,男女比例9:4)。所有患者均有头颈部病变。75.0%的患者外周血嗜酸性粒细胞升高,77.8%的患者外周血嗜酸性粒细胞百分比升高,所有患者IgE水平均升高。治疗包括手术切除、糖皮质激素、甲氨蝶呤、低剂量放疗和观察。76.9%的患者获得缓解。结果较差的患者绝对嗜酸性粒细胞计数(中位数:1.77 vs. 0.90 × 10⁹/L, p = 0.04)和百分比(中位数:21.4% vs. 12.2%, p = 0.03)显著高于结果良好的患者。影像学误诊率为38.5%,凸显了组织病理学诊断的优越性。尿异常、轻度肾功能不全和罕见病变部位也被观察到。结论:KD的临床异质性需要多学科管理。治疗前嗜酸性粒细胞增多症正在成为一种预后指标。未来的研究应优先考虑生物标志物的鉴定、动力学监测和靶向生物制剂,以减少复发和全身并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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