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Symmetrical acrokeratoderma: a case series in Indian patients
Keshavamurthy Vinay1, Gitesh U Sawatkar1, Uma N Saikia2
1Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India.
Orphanet Journal of Rare Diseases
|November 24, 2016
Summary
Symmetrical acrokeratoderma, a rare skin condition, presents as brownish-black plaques on hands and feet in young adult males. This Indian case series highlights its clinical features and response to treatment.
Area of Science:
- Dermatology
- Clinical Medicine
Background:
- Symmetrical acrokeratoderma is a recently identified dermatosis primarily affecting young adult males of Chinese descent.
- This report details five cases of symmetrical acrokeratoderma observed in India, expanding the known geographical distribution of the condition.
Observation:
- Patients presented with asymptomatic, brownish-black plaques symmetrically distributed on the dorsum of hands and feet.
- Lesions characteristically spared palms and soles, showed whitish maceration upon water immersion, and worsened in hot, humid climates.
- Variable involvement of wrists, forearms, elbows, ankles, shins, and knees was noted.
Findings:
- Histopathology revealed basket weave hyperkeratosis, irregular acanthosis, and mild perivascular lymphomononuclear infiltrate.
- Biopsies post-immersion demonstrated loosening of the stratum corneum.
- Acitretin offered short-term symptomatic relief but did not alter the long-term disease course.
Implications:
- This study broadens the understanding of symmetrical acrokeratoderma's clinical presentation and geographical occurrence.
- Further research is needed to elucidate the genetic and environmental factors contributing to the causation of this dermatosis.
- Identifying causative factors is crucial for developing targeted and effective long-term treatment strategies.
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