Idiopathic eruptive macular pigmentation (IEMP) is a rare condition which was described in 1978 by French doctors Degos et al. 1 The first reference in the English literature was in 1996; Sanz de Galdeano et al. 2 summarized the diagnostic criteria after collecting and observing five cases: (1) eruption of brownish, nonconfluent, asymptomatic macules involving the trunk, neck, and proximal extremities in children or adolescents; (2) absence of preceding inflammatory lesions; (3) no prior drug exposure; (4) basal cell layer hyperpigmentation of the epidermis and prominent dermal melanophages without visible basal layer damage or lichenoid inflammatory infiltrate; and (5) normal mast cell count. The pathogenesis of IEMP remains unclear. It seems that sunlight is not important, as most lesions occur in photoprotected areas. 3 And there have been no reported cases of IEMP with a family history. 4 F I G U R E 1 Multiple, brown, non-scaly macules and patches. (A) Abdomen, (B) waist, (C) upper arm, (D) upper legs This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.