| Jackson-Lawler综合征1例 |
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| 引用本文： | 李会申,张文娟,崔树岩,孙祎山,苏燕晨. Jackson-Lawler综合征1例[J]. 临床皮肤科杂志, 2004, 33(1): 28-29 |
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| 作者姓名： | 李会申 张文娟 崔树岩 孙祎山 苏燕晨 |
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| 作者单位： | 北京大学人民医院皮肤科,北京,100044 |
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| 摘 要： | 报告1例Jackson-Lawler综合征。患儿男，10岁。自出生后3个月起双手、足指（趾）甲增厚，伴面部、躯干、四肢丘疹和结节。甲真菌检查阴性，皮肤组织病理检查证实为多发性脂囊瘤，临床诊断为Jackson-Lawler综合征。
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| 关 键 词： | Jackson-Lawler综合征 |
| 文章编号： | 1000-4963(2004)01-0028-02 |
| 修稿时间： | 2003-03-10 |
Jackson-Lawler syndrome:a case report |
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| LI Hui-shen,ZHANG Wen-juan,CUI Shu-yan,SUN Wei-shan,SU Yan-chen. Jackson-Lawler syndrome:a case report[J]. Journal of Clinical Dermatology, 2004, 33(1): 28-29 |
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| Authors: | LI Hui-shen ZHANG Wen-juan CUI Shu-yan SUN Wei-shan SU Yan-chen |
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| Abstract: | A case of Jackson-Lawler syndrome is reported. The patient was a 10-year-old boy. He had thick nails since he was 3 months old. Physical examination revealed hypertrophic nails of all fingernails and toenails , papules and nodules on his face, neck, trunk and extremities. Histology of the skin nodule showed a characteristic of steatocystoma multiplex.The mycologic examination of nails was negative. He was diagnosed as Jackson-Lawler syndrome. |
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| Keywords: | Jackson-Lawler syndrome |
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