期刊文献+

遗传性半透明性丘疹性肢端角化症二例

Hereditary papulotranslucent acrokeratoderma: two cases report
下载PDF
导出
摘要 遗传性半透明性丘疹性肢端角化症是一种罕见的发生于掌跖部位,表现为黄白色半透明丘疹的皮肤病,本病多有家族史,但亦存在散发病例。本文报道2例散发性病例,患者均为中青年女性,青少年时期发病,双手累及,临床症状典型,治疗效果均不甚理想。 Hereditary papulotranslucent acrokeratoderma is a rare disease, usually with a family history, characterized by yellowish white and translucent papules on palms and soles. The disease usually has a family history, but there are still some sporadic cases. Two sporadic cases were reported, both were young and middle-aged women. The disease developed in adolescence and involved hands, and the clinical symptoms of which were typical, but the effectiveness of the treatment was not satisfactory.
作者 何婷婷 顾海萍 贾虹 HE Ting-ting;GU Hai-ping;JIA Hong(Nanjing University of Traditional Chinese Medicine, Nanjing 210023, China)
出处 《实用皮肤病学杂志》 2018年第3期181-182,185,共3页 Journal of Practical Dermatology
关键词 肢端角化症 遗传性 Acrokeratoderma hereditary
  • 相关文献

参考文献1

二级参考文献4

  • 1Onwukwe MF,Mihm MC Jr, Toda K. Hereditary papulotranslu-cent acrokeratoderma: a new variant of familial punctate kerato-derma[J]. Arch Dermatol, 1973, 108(1): 108-110.
  • 2倪启超,朱根悌.遗传性半透明丘疹性指端角化症孪生兄弟2例报告[J].中国皮肤性病学杂志,1996,10(2): 98.
  • 3Sracic JK, Krishnan RS, Nunez-Gussman JK, et al. Hereditarypapulotranslucent acrokerato-derma: a case report and literaturereview[J]. Dermatol Online J, 2005, 11(3): 17.
  • 4Rizzo C, Bragg J,Soldano AC, et al. Hereditary papulotranslu-cent acrokeratoderma[J]. Dermatol Online J, 2008, 14(5): 3.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部