Dominant dystrophic epidermolysis bullosa

Hae Jin Lee, Ye Jin Jung, Jae Hong Kim, Hannah Hong, Eung Ho Choi

Research output: Contribution to journalArticle

Abstract

Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease with a hereditary pattern of occurrence, and this disease easily produces bullae that heal with scarring and milium formation. A 13-month-old female baby was brought to the department of dermatology with multiple variable sized bullae and erythematous to dark brownish patches and crusts on both her feet. The histopathologic findings showed subepidermal non-inflammatory blisters and the electron microscopic findings showed vacuolization of the sublamina densa and broken anchoring fibrils. On the basis of the clinical and microscopic findings, she was diagnosed as having dominant dystrophic epidermolysis bullosa. We report here on a case of dominant dystrophic epidermolysis bullosa with the clinical, histological and electron microscopic findings, as well as the family history of the patient.

Original languageEnglish
Pages (from-to)889-892
Number of pages4
JournalKorean Journal of Dermatology
Volume48
Issue number10
Publication statusPublished - 2010 Oct 1

All Science Journal Classification (ASJC) codes

  • Dermatology

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    Lee, H. J., Jung, Y. J., Kim, J. H., Hong, H., & Choi, E. H. (2010). Dominant dystrophic epidermolysis bullosa. Korean Journal of Dermatology, 48(10), 889-892.