“…Atypical and rare variants [45] include the folliculotropic MF (FMF)/syringotropic forms [24,78,126,127] accounting for about 10-15% of the total MF cases, the chalazoderma-type MF, also termed granulomatous slack skin [76], pagetoid reticulosis, ichthyosiform MF [87], blastic MF, granulomatous MF [60,128], hypopigmented MF, useful considered as a surrogate marker of cytotoxic immunity targeting the malignant T cells and papillomatous MF, verrucous MF [104], poikilodermic MF [100-102, 132], and invisible MF where pruritus is the only clinical sign [24,93,118]. All these aforementioned clinical subtypes of MF may imitate a large array of other dermatological manifestations [6, 26,27,31,[133][134][135], again hindering prompt diagnosis. This fact has already been described [133], relating that MF can mimic more than 50 different clinical entities.…”