Differential diagnosis
Punctate keratoses of the palms are fairly common frequently overlooked lesions. The differential diagnosis is extensive (Table), but there are several clinical features of KPPC that distinguish it from other hyperkeratotic conditions. The lesions of KPPC can be painful, have a predilection for jointcreases, and evolve into pits.3 KPPP is similar except not localized to the creases.4
Aquagenic keratoderma is a transitory condition afflicting young women and defined clinically by the appearance of palmar lesions accentuated after immersion in water. These lesions have a characteristic histological appearance (hyperkeratosis, dilated eccrine ducts).13
Palmoplantar pustulosis is characterized by chronically recurring sterile pustules on the palms and soles, usually found on an erythematous base, and a strong association with tobacco use.14Palmoplantar lichen planus may exhibit a variety of morphologic patterns including papules or plaques with pruritus, erythema, and compact hyperkeratosis.15
Cole disease is an uncommon disorder typified by distinctive cutaneous hyperpigmentation and punctate keratoses on the palms and soles. It is a congenital disease with an autosomal dominant inheritance pattern and phenotypic variability.16
Palmoplantar psoriasis is associated with manual labor in 50% of cases. Lesions are restricted to areas exposed to pressure. All patients with unilateral palmar lesions had them on their dominant hand. Biopsy may be necessary to differentiate hyperkeratotic eczema from psoriasis when just localized to the palms and soles.17
TABLE
Differential diagnosis of punctate keratoses of the hands and feet
Acquired keratoses | Classic clinical description | Associations |
---|---|---|
Arsenical | Round, verrucous, or acuminate keratotic papules most common on palms and soles. Typically occur decades after chronic arsenic ingestion | Angiosarcoma of the liver, nonmelanoma skin cancer, bronchial adenocarcinoma |
Idiopathic filiform porokeratoses | Multiple thin spiny keratotic projections on palms and soles | Breast, renal, colon, and lung cancer |
Keratosis punctata of the palmar creases | Discrete, sharply marginated, hyperkeratotic, conical, 1–5 mm depressions confined to flexural creases | Dupuytren’s contracture, striate keratoderma, knuckle pads |
Hereditary keratoses | Classic clinical description | Associations |
Keratosis punctata palmoplantaris (type I), Buschke-Fischer-Brauer disease | Multiple 1–2 mm punctate keratoses of the palms and soles | Longitudinal nail dystrophy, lichen nitidus, ichthyosis, atopy, recalcitrant warts. Increased risk of malignancy |
Spiny keratoderma (type II) | Small keratotic spines over entire palmoplantar surfaces. Resembles the spines of an old-fashioned music box | No predisposition to malignancy |
Acrokeratoelastoidosis lichenoids (type III) | 2–4 mm round to oval papules on the borders of hands, feet and wrists. May be umbilicated and become confluent | Darier’s disease, Cowden’s disease |
Adapted from Rustad et al 1990,5 Kong et al 2004,7 Asadi 2003,9 Habif 2004,11 and Osman et al 1992.12 |