...
首页> 外文期刊>Journal of cutaneous medicine and surgery >A Rare Case of Solitary Giant Congenital Juvenile Xanthogranuloma: A Case Report
【24h】

A Rare Case of Solitary Giant Congenital Juvenile Xanthogranuloma: A Case Report

机译:少数孤独巨型先天性青少年Xanthogranuloma:案例报告

获取原文
获取原文并翻译 | 示例

摘要

Juvenile xanthogranuloma (JXG) is the most frequent form of non-Langerhans cell histiocytosis. We present a case of giant congenital JXG in a 7-week-old boy, who had a firm and incompressible lesion, measuring 3 x 4 cm in diameter, on his right flank. The clinical appearance of the lesion and the ultrasound results suggested a vascular tumor, such as a hemangioma. Histology confirmed a JXG, although there was an absence of Touton cells, which are usually pathognomonic of JXG. In light of these findings, it would be important to include JXG in the differential diagnosis of congenital tumours, particularly vascular lesions.
机译:青少年Xanthogranuloma(JXG)是最常见的非朗格汉斯细胞组织细胞毒性形式。 我们在一个7周龄男孩中提出了一个巨大的先天性JXG,他有一个坚定的韧性和不可压缩的病变,直径为3×4厘米,在他的右侧。 病变和超声结果的临床外观表明血管肿瘤,例如血管瘤。 组织学证实了JXG,尽管没有Touton细胞,这通常是JXG的公开。 根据这些发现,重要的是在先天性肿瘤的差异诊断中包含JXG,特别是血管病变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号