中国麻风皮肤病杂志 ›› 2020, Vol. 36 ›› Issue (12): 741-743.doi: 10.12144/zgmfskin202012741

• 病例报告 • 上一篇    下一篇

黄色肉芽肿样单发型朗格汉斯细胞组织细胞增生症一例

黄春兰,郑惠文,李寅,李薇,郭小璇,周沙,李云玲   

  1. 浙江大学医学院附属儿童医院（国家儿童健康与疾病临床医学研究中心）皮肤科,杭州，310052
  • 出版日期:2020-12-15 发布日期:2020-12-04
  • 通讯作者: 李云玲，E-mail: liyunling@zju.edu.cn

Solitary Langerhans cell histiocytosis manifested by xanthogranulomatous lesions: a case report

HUANG Chunlan, ZHENG Huiwen, LI Yin, LI Wei, GUO Xiaoxuan, ZHOU Sha, LI Yunling   

  1. Department of Dermatology, The Children's Hospital, Zhejiang University School of Medicine,  National Clinical Research Center for Child Health, Hangzhou 310052, China
  • Online:2020-12-15 Published:2020-12-04
  • Contact: LI Yunling, E-mail: liyunling@zju.edu.cn

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摘要： 朗格汉斯细胞组织细胞增生症（Langerhans cell histiocytosis, LCH）是一种少见的病因不明的疾病，表现为单发型皮损的朗格汉斯细胞组织细胞增生症更是罕见,本文报道一例。该患儿7个月，表现为右侧肩部单发黄红色结节2个月，皮损与黄色肉芽肿非常相似，极易误诊为黄色肉芽肿。

关键词: 朗格汉斯细胞组织细胞增生症, 单发, 皮肤型

Abstract:

Langerhans cell histiocytosis (LCH) is a rare group of disorders without a well-understood etiology and solitary is more rare. We report a case with solitary Langerhans cell histiocytosis in this paper. A 7-month-old patient presented with a yellowish red nodule, very similar to xanthogranuloma lesion, on the right shoulder for 2 months.

Key words: Langerhans cell histiocytosis, solitary, cutaneous