“…Clinically, MF typically presents with cutaneous erythematous patches, plaques, tumors, or erythroderma. Nevertheless, atypical variants of MF exist that vary considerably in their clinical and histological features and prognosis: folliculotropic, pagetoid reticulosis, granulomatous slack skin, bullous, hypopigmented, ichthyosiform, pigmented purpuric dermatosis-like, papular, poikilodermatous, psoriasiform, pustular, and verrucoid [ 7 , 8 , 9 , 10 , 11 ]. Consequently, the diagnosis of MF is often difficult and challenging: the differential diagnosis is wide, and the histological findings may be non-specific in the early stages.…”