| 先天性角化不良2例 |
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| 引用本文： | 王建琴,许剑荣,孙广政,刘衍彬,唐绍生. 先天性角化不良2例[J]. 中国皮肤性病学杂志, 2002, 16(4): 260-262 |
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| 作者姓名： | 王建琴 许剑荣 孙广政 刘衍彬 唐绍生 |
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| 作者单位： | 广州市第一人民医院皮肤科,广东广州,510180 |
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| 摘 要： | 先天性角化不良是一种罕见的多系统疾病，主要累及中胚层和外胚层，约80％以上的患者发生骨髓衰竭，并于早期死亡。报告2例患者，1例为22岁男孩，另1例为16岁女孩，均具有网状色素沉着伴毛细血管扩张及皮肤萎缩、甲营养不良、黏膜白斑等典型临床表现。男性患者伴有血液系统异常。
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| 关 键 词： | 先天性角化不良 临床分析 骨髓衰竭 |
| 文章编号： | 1001-7089(2002)04-0260-03 |
| 修稿时间： | 2001-11-27 |
Two Cases of Dyskeratosis Congenita |
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| WANG Jian qin,XU Jian rong,SUN Guang zheng,et al. Two Cases of Dyskeratosis Congenita[J]. The Chinese Journal of Dermatovenereology, 2002, 16(4): 260-262 |
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| Authors: | WANG Jian qin XU Jian rong SUN Guang zheng et al |
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| Affiliation: | WANG Jian qin,XU Jian rong,SUN Guang zheng,et al Department of Dermatology,First Municipal People's Hospital of Guangzhou,Guangzhou 510180,China |
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| Abstract: | Dyskeratosis congenita is a rare multi system disease mainly involving mesoblast and ectoderm.We report 2 cases of dyckeratosis congenita,one was a 22 year old boy,another was a 16 year old girl.Both of them presented characteristic clinical symptoms,such as reticular skin pigmentation,nail dystrophy and leukoplakia of mucous membranes,etc.The male patient also accompanied with abnormalities of blood system. |
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| Keywords: | Dyskeratosis congenita |
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