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  Vol. 134 No. 4, April 1998 TABLE OF CONTENTS
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Persistent, Solitary, Erythematous, Hyperkeratotic Plaque

Neville G. Pereyo, MD; Omar P. Sangueza, MD; Loretta S. Davis, MD
Medical College of Georgia, Augusta

Arch Dermatol. 1998;134:499-504.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

REPORT OF A CASE

A 52-year-old white woman presented with a pruritic, scaly lesion on her right forearm that had been present for several months. Her medical and family histories were unremarkable.

The physical examination revealed a 5x6-mm, well-circumscribed, erythematous plaque on the dorsal aspect of the right forearm (Figure 1). The lesion was treated twice with cryosurgery and subsequently with diflorasone diacetate cream, but persisted despite these measures. A 4-mm punch biopsy specimen of the lesion revealed epidermal hyperplasia with compact hyperkeratosis and acanthosis. In the stratum spinosum and granulosum, there were vacuolar and granular changes with coarse, prominent keratohyaline granules. The dermis showed prominent solar elastosis (Figure 2).


Figure 1.


Figure 2.

What is your diagnosis?


DIAGNOSIS: Isolated epidermolytic acanthoma (IEA).

Isolated epidermolytic acanthoma was first described in 1970 by Shapiro and Baraf1 as an acquired, solitary lesion showing . . . [Full Text of this Article]



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Lipedematous Alopecia in a White Woman
Tiscornia et al.
Arch Dermatol 2002;138:1517-1518.
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