“…Clinically, the characteristic eruption of IEMP is composed of round to oval, circumscribed, non-pruritic, homogeneous pigmented macules and plaques that appear without previous erythematous, papular, or hypochromic lesions, occurring mostly on the trunk, neck, and proximal portion of the extremities. However, lesions occurring in a Christmas tree pattern and limited to flexural areas of the body have also been documented in the literature [18,19]. IEMP needs to be differentiated clinically and histologically from friction melanosis, post-inflammatory hyperpigmentation, fixed drug eruption (FDE), urticaria pigmentosa, lichen planus pigmentosus (LPP), erythema dyschromicum perstans (EDP), pigmentary disorders that involve the flexural areas like Dowling-Degos disease and acanthosis nigricans as these conditions can cause diagnostic conundrum and unnecessary therapeutic interventions [13,19].…”