Kyeong Jin Lee, Ha Young Lee, Suk Jin Choi, Myung Kwan Lim, Young Hye Kang
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引用次数: 0
Abstract
Kimura's disease (KD) is a rare, chronic inflammatory disorder characterized by angiolymphoid hyperplasia, peripheral eosinophilia, and elevated serum immunoglobulin E levels. It primarily affects young Asian males and typically involves the head and neck region, especially near the mandible and postauricular regions. Orbital involvement is unusual and extraocular muscle (EOM) involvement is exceedingly rare, with only a few cases reported in the literature. The present report describes a case of surgically confirmed KD in a 16-year-old male, involving the bilateral EOM, lacrimal gland, and left parotid gland.
木村氏病(KD)是一种罕见的慢性炎症性疾病,以血管淋巴细胞增生、外周嗜酸性粒细胞增多和血清免疫球蛋白 E 水平升高为特征。它主要影响年轻的亚洲男性,通常累及头颈部,尤其是下颌骨和耳后附近。眼眶受累并不常见,眼外肌(EOM)受累则极为罕见,文献中仅有几例报道。本报告描述了一例经手术确诊的KD病例,患者为一名16岁男性,双侧眼外肌、泪腺和左侧腮腺均受累。