Korean J Dermatol.  1994 Jun;32(3):518-522.

A Case of Epidermolysis Bullosa Dystrophica Dominant

• Jung MJ
• Lee JS
• Kim YK

Abstract

Epidermolysis bullosa dystrophica is rare, chronic non-inflammtory mechanobullous disease of hereditary trait, which easily produces bullae by minor trauma or sponta neosly. A 1-day old male neonate presented wide spread vesicobullous minor, eruptions since birth. On examination, tense bullse were noted on the dorsa of the feet and right knei: area Which is usually serous but may be hemarrhagic tendeney. This was healed by the dropping of oxoline and wet betadine auze application along with the administration of vitamin E and phenytoin. We present a case of epidermolysis bullosa dystrophica that seems be a dominant type considering the presence of family history with histopathologic and electron microscopic findings.

Keyword

Epidermolysis Bullosa Dystrophica Dominant

MeSH Terms

Epidermolysis Bullosa Dystrophica*
Epidermolysis Bullosa*
Foot
Humans
Infant, Newborn
Male
Parturition
Phenytoin
Povidone-Iodine
Transcutaneous Electric Nerve Stimulation
Vitamin E
Vitamins
Phenytoin
Povidone-Iodine
Vitamin E
Vitamins