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Palmoplantar keratoderma of punctate type: acrokeratoelastoidosis Costa
Acta Dermato-Venereologica
|January 1, 1980
Summary
This study describes a rare hereditary palmoplantar keratoderma in Finnish families, presenting as symptomless papules. The condition, likely acrokeratoelastoidosis Costa, suggests an autosomal dominant inheritance pattern.
Area of Science:
- Dermatology
- Genetics
- Histopathology
Background:
- Punctate palmoplantar keratoderma is a rare condition affecting the palms and soles.
- A specific variant observed in Finnish families presented unique clinical and histological features.
Purpose of the Study:
- To clinically, histologically, and ultrastructurally characterize a distinct form of punctate palmoplantar keratoderma.
- To investigate the inheritance pattern and potential associations of this condition.
Main Methods:
- Clinical examination of 10 patients from six Finnish families.
- Histological and ultrastructural analysis of skin lesions.
- Pedigree analysis to determine inheritance patterns.
Main Results:
- Patients exhibited symptomless, transparent, hyperkeratotic papules on palms, fingers, wrists, and soles.
- Histology showed undulating hyperkeratosis; ultrastructural analysis revealed deep dermal elastic fiber alterations.
- Autosomal dominant inheritance was suggested, with some patients presenting knuckle pads and recalcitrant warts.
Conclusions:
- The described condition is considered a variant of acrokeratoelastoidosis Costa.
- This variant of hereditary palmoplantar keratoderma has distinct clinical and ultrastructural findings.