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作 者:任发亮[1] 谭琦[1] 甘立强[1] 陈光华[1] 方晓[1] 侯倩[1] 王华[1] REN Fa-liang;TAN Qi;GAN Li-qiang;CHEN Guang-hua;FANG Xiao;HOU Qian;WANG Hua(Department of Dermatology,Children's Hospital of Chongqing Medical University,Ministry of Education Key Laboratory of Child Development and Disorders,China International Science and Technology Cooperation base of Child development and Critical Disorders,Chongqing Key Laboratory of Pediatrics,Chongqing 400014,China)
机构地区:[1]重庆医科大学附属儿童医院皮肤科儿童发育疾病研究教育部重点实验室儿童发育重大疾病国家国际科技合作基地儿科学重庆市重点实验室,重庆400014
出 处:《临床皮肤科杂志》2018年第9期568-570,共3页Journal of Clinical Dermatology
摘 要:患儿女,13岁。躯干左侧带状褐色斑片7年。皮肤科检查:躯干左侧可见两条沿Blaschko线分布呈倒"S"形的淡红褐色萎缩性带状斑片。皮损组织病理:表皮中央部分轻度萎缩变薄,基底层黑素增加。诊断:儿童Moulin线状萎缩性皮病。An 11-year-old girl presented with asymptomatic hyperpigmented atrophic patches on the left trunk for 7 years. Otherwise the girl was normal. Dermatological examination showed two reddish-brown, atrophic banded patches with an inverted "S" shape along the Blaschko's lines on the left side of the trunk. Histopathology showed mild atrophy and thinning of the middle epidermis, and increased pigment in the basal layer. Verhoeff-Van Gleson staining showed normal elastic fibers in the dermis. Children's linear atrophodenna of Moulin was diagnosed.
分 类 号:R758.56[医药卫生—皮肤病学与性病学]
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