| Autor: |
Vora, Rita Vipul, Diwan, Nilofar Gulamsha, Jivani, Nidhi B., Singhal, Rochit Rajesh, Gandhi, Shailee Sanjay |
| Předmět: |
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| Zdroj: |
Medical Journal of Dr. D.Y. Patil University; Mae/Apr2017, Vol. 10 Issue 2, p195-197, 3p |
| Abstrakt: |
Acrokeratosis verruciformis (AKV) of Hopf is an autosomal dominant condition characterized by multiple flesh-colored or lightly pigmented flat or convex warty papules over dorsa of hands, feet, knees, elbows, and forearms. It affects both sexes and is usually present at birth or appears in early childhood. Two forms of the disease have been described, namely, classical AKV and sporadic AKV. Histological examination differentiates it from other similar conditions. Superficial ablation is the treatment of choice. We represent a case of a young female with extensive lesions over contralateral limbs, of classical AKV interspersed with multiple hypopigmented macular lesions of AKV. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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