Lenne Y, Gaillard A, Bonnard J, Billet J, Fiche M, Gordeeff A, Ayoun G
Rev Stomatol Chir Maxillofac. 1985;86(6):378-81.
A rare affection of unknown etiology that is benign but frequently recurrent, Kimura's disease involves infiltration of the dermis and hypodermis usually of the face. Documented data exists describing clinical findings and results of histopathology that are analogous but are grouped under other names: angiolymphoid hyperplasia with eosinophilia, pyogenic pseudogranuloma, atypical pyogenic granuloma. A case followed up for 13 years is reported.
木村病是一种病因不明的罕见疾病,呈良性但常复发,通常累及面部真皮和皮下组织。现有文献资料描述了类似的临床表现和组织病理学结果,但被归在其他名称之下:嗜酸性粒细胞增多性血管淋巴样增生、化脓性假肉芽肿、非典型化脓性肉芽肿。本文报告了一例随访13年的病例。