Marginal papular acrokeratodermas (MPA) are a group of disorders that have keratotic papules along the borders of the hands and feet as a common clinical feature [1]. Acrokeratoelastoidosis (AKE) and focal acral hyperkeratosis (FAH) are rare clinical variants of MPA [2,3]. We herein report a sporodic AKE in a 62 year-old female and a sporodic FAH in a 41-year-old female.

Acrokeratoelastoidosis was first described by Costa in 1953 [2]. In 1983 Dowd and et al. described fifteen patients clinically identical to acrokeratoelastoidosis, but without elastorrhexis. This condition which differs histologically from AKE was named FAH [4]. They suggested that FAK is a focal disorder of keratinization of unknown etiology rather than a disease of the elastic fibers as in acrokeratoelastoidosis [2]. However, some authors consider FAH to be a distinct entity or others think that FAH is a variant of AKE [1,5-7]. Both disorders are either sporadic or familial, with an apparent autosomal dominant inheritance [2,3,8]. Our both cases were sporadic.

Clinically, both conditions are characterized by asymptomatic, multiple, small, shiny, smooth, firm, and yellowish papules, sometimes umbilicated, located symmetrically on both thenar and hypothenar regions, the volar aspect of the wrist, dorsa and sides of the digits, and radial and ulnar margins of the hands. The dorsa of the feet and toes, and soles may also be affected [5]. Clinically, these two similar entities were distinguished by histopathological features. Histologically AKE and FAH both show orthohyperkeratosis overlying a crateriform depression in the epidermis. However, FAH lacks elastorrhexis, a major distinguishing feature between the two [3]. Our both cases showed similar clinic presentation. Histopathologically, our first case showed elastorrhexis but our second case showed no elastorrhexis. According to these findings, our first case was diagnosed as AKE and our second case was diagnosed as FAH.

AKE and FAH must be differentiated from verruca plana, acrokeratosis verruciformis of Hopf, degenerative collagenous plaques of the hands, digital papular calcinosis, mosaic acral keratosis, and hereditary papulotranslucent acrokeratoderma punctate porokeratosis and punctate palmoplantar keratoderma [3,6,8].

AKE and FAH have been rarely reported in the English literature with unkown etyology. Clinical and histopathological findings are the most important tools to define diagnosis and distinguish the other keratinization disorders. Additional case reports and further genetic studies are requaried to more understanding of the diseases.