Related Experiment Videos
Transient reactive papulotranslucent acrokeratoderma associated with cystic fibrosis
M A Lowes1, G S Khaira, D Holt
1Dermatology Department, Royal Newcastle Hospital, Australia. malowes@enternet.com.au
The Australasian Journal of Dermatology
|August 24, 2000
Summary
A rare skin condition, transient reactive papulotranslucent acrokeratoderma, was observed in a cystic fibrosis patient. This finding suggests a potential link between cystic fibrosis and this specific type of keratoderma.
Area of Science:
- Dermatology
- Genetics
- Internal Medicine
Background:
- Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs.
- Punctate keratodermas are a group of inherited skin conditions characterized by small, horny papules.
- Transient reactive papulotranslucent acrokeratoderma is a recently identified condition with unknown triggers.
Observation:
- A 20-year-old female with a known diagnosis of cystic fibrosis presented with a distinct palmar skin eruption.
- The eruption consisted of white papules on the palms, appearing after water exposure.
- No prior family history of keratoderma was reported in the patient.
Findings:
- Biopsy revealed hyperkeratosis (thickened skin) surrounding dilated eccrine ostia (sweat gland openings).
- The histological features were consistent with transient reactive papulotranslucent acrokeratoderma.
- This represents the first reported association between cystic fibrosis and this specific keratoderma variant.
Implications:
- The findings suggest a potential, previously undescribed association between cystic fibrosis and transient reactive papulotranslucent acrokeratoderma.
- Further research may elucidate the underlying mechanisms connecting CFTR dysfunction to this skin manifestation.
- This case expands the clinical spectrum of skin conditions associated with cystic fibrosis.