【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。更多还原

【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.更多还原