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KMID : 0363219940320030518
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Korean Journal of Dermatology
1994 Volume.32 No. 3 p.518 ~ p.522
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A Case of Epidermolysis Bullosa dystrophica dominant
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Abstract
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Epidermolysis bullosa dystrophica is rare, chronic non-inflammatory mechanobullous disease of hereditary trait, which easily produces bullae by minor trauma or spontaneosly.
A 1-day old male neonate presented wide spread vesicobullous skin eruptions since birth. On examination, tense bullae were noted on the dorsa of the feet and right knee area which is usually serous but may be hemorrhagic tendency.
This was healed by the dropping of oxoline and wet betadine gauze application along with the administration of vitamin E and phenytoin.
We present a case of epidermolysis bullosa dystrophica that seems to be a dominant type considering the presence of family history with histopathologic and electron microscopic findings. (Kor J Dermatol 1994 ; 32(3) : 518~522)
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