A Case of Epidermolysis Bullosa Hereditaria

Hiromichi Takeshita, Masutaka Furue, Hiromaro Kiryu

研究成果: Contribution to journalArticle査読

抄録

A newborn male with, recessive dystrophic epidermolysis bullosa hereditaria is presented. The patient developed excoriation, blisters, erosion, and milia formations mainly on his extremities after birth. Histopathologically. sections from the eroded skin revealed a loss of the epidermis and probable subepidermal blister formation as evidenced by the presence of preserved dermal papillae associated with mild lymphocytic infiltrate in the dermis. He was treated with oral tocopherol acetate and phenytoin from the fifth day after birth. However, this therapy proved to be ineffective. In addition, he also developed progressive fusion of the toes by severe scarring with a loss of his toe nails.

本文言語英語
ページ(範囲)754-756
ページ数3
ジャーナルNishinihon Journal of Dermatology
60
6
DOI
出版ステータス出版済み - 1 1 1998

All Science Journal Classification (ASJC) codes

  • 皮膚病学

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