Cusick E L, Spicer R D
Bristol Childrens Hospital, UK.
Eur J Pediatr Surg. 1994 Dec;4(6):368-9. doi: 10.1055/s-2008-1066137.
Juvenile xanthogranuloma (JXG) is a rare affliction of early childhood comprising cutaneous and deep-seated lesions. Accurate diagnosis is important as the condition is self-limiting with spontaneous regression over a period of months. A case of congenital JXG is reported and the literature briefly reviewed.
幼年性黄色肉芽肿(JXG)是一种儿童早期的罕见疾病,包括皮肤和深部病变。准确诊断很重要,因为这种疾病具有自限性,会在数月内自然消退。本文报告了一例先天性JXG病例,并对相关文献进行简要综述。