[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address Please contact the publisher to request reinstatement.
[Skip to Content Landing]
May 1995

Acantholytic Epidermolysis Bullosa

Author Affiliations

From the Department of Dermatology, Rush-Presbyterian-St Luke's Medical Center, Chicago, Ill.

Arch Dermatol. 1995;131(5):586-589. doi:10.1001/archderm.1995.01690170088013

Background:  We describe a new variant of inherited epidermolysis bullosa and elucidate the clinical, histologic, and ultrastructural features of this condition.

Observations:  This form of epidermolysis bullosa displays an autosomal dominant inheritance pattern, is characterized by acral bullae, and histologically demonstrates suprabasal clefting with acantholysis. Ultrastructural findings are nonspecific but reminiscent of those observed in benign familial pemphigus.

Conclusion:  Acantholytic epidermolysis bullosa is a rare but distinct clinicopathologic entity that warrants inclusion in the nosologic classification of epidermolysis bullosa.(Arch Dermatol. 1995;131:586-589)