Choi Won Jun, Hur Jae, Ko Joo Yeon, Yeo Kwang Yeoll, Kim Joung Soo, Yu Hee Joon
Department of Dermatology, College of Medicine, Hanyang University, Seoul, Korea.
Ann Dermatol. 2010 Feb;22(1):57-60. doi: 10.5021/ad.2010.22.1.57. Epub 2010 Feb 28.
Kimura's disease is a rare inflammatory disorder of unknown etiology primarily seen in young Asian males. It is characterized by painless subcutaneous masses, blood and tissue eosinophilia, and markedly elevated serum immunoglobulin E (IgE) levels. Clinically, the subcutaneous nodules occur predominantly in the head and neck. However, we report the case of a five-year-old boy presenting with an asymptomatic solitary brown pigmented nodule on the left buttock diagnosed with Kimura's disease. Here we describe the diagnosis and treatment of this unusual case.
木村病是一种病因不明的罕见炎症性疾病，主要见于年轻亚洲男性。其特征为无痛性皮下肿块、血液和组织嗜酸性粒细胞增多，以及血清免疫球蛋白E（IgE）水平显著升高。临床上，皮下结节主要发生在头颈部。然而，我们报告了一例5岁男孩的病例，该男孩左侧臀部出现一个无症状的孤立性褐色色素沉着结节，诊断为木村病。在此，我们描述该罕见病例的诊断和治疗。
