Uysal Ismail O, Eryilmaz Mehmet A, Salk Ismail, Abasiyanik Fatma
Department of Otorhinolaryngology, Cumhuriyet University School of Medicine, Sivas, Turkey.
J Craniofac Surg. 2011 Jan;22(1):337-8. doi: 10.1097/SCS.0b013e3181f7e0cc.
Kimura disease (KD) is a rare entity that occurs primarily in Asian people characterized histopathologically by a lymph-folliculoid granuloma with infiltration of the mass and the surrounding tissues by eosinophils, often with concomitant peripheral blood eosinophilia and elevated serum immunoglobulin E, generally seen in the head and neck region, especially preauricular area. In this article, we present the case of a 14-year-old male patient with KD on his left parotid area. The clinical, radiologic, surgical, and pathologic findings of KD are discussed in this article.
木村病（KD）是一种罕见疾病，主要发生于亚洲人群，其组织病理学特征为淋巴滤泡样肉芽肿，肿块及周围组织有嗜酸性粒细胞浸润，常伴有外周血嗜酸性粒细胞增多和血清免疫球蛋白E升高，多见于头颈部区域，尤其是耳前区。在本文中，我们报告了一例14岁男性左侧腮腺区患木村病的病例。本文讨论了木村病的临床、影像学、手术及病理表现。
