伴有皮肤外病变的幼年性黄色肉芽肿——病例报告

Juvenile xanthogranuloma with extra-cutaneous lesions--a case report.

作者信息

Cusick E L, Spicer R D

机构信息

Bristol Childrens Hospital, UK.

出版信息

Eur J Pediatr Surg. 1994 Dec;4(6):368-9. doi: 10.1055/s-2008-1066137.

DOI:10.1055/s-2008-1066137

PMID:7748839

Abstract

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.

摘要

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。