Abstract
Poikiloderma vasculare atrophicans (PVA), also known as parakeratosis variegata, is considered a rare variant of early-stage mycosis fungoides or a premycotic condition usually presenting as asymptomatic or moderately pruritic, mildly scaling, reddish-brown papules, often coalescing into net-like patterned lesions, which mainly involve the breast, abdomen, buttocks, and flexures [1, 2]. Although the diagnosis of this condition is usually straightforward, sometimes the distinction from other similar [...]
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