“…Diagnosis is usually clinical, but diagnostic skin biopsy is recommended in case of multiple lesions to rule out other pathologic processes. Histology shows dense, well-demarcated dermal lymphohistiocytic infiltration interlaced with giant cells, and immunohistochemistry positive for macrophage markers (CD68, CD163, KiM1P, anti-FXIIIa, vimentin and anti-CD4) and negative for S100, CD1a and CD207, specific for Langerhans cells [2][3][4] . Differential diagnosis, mainly in multiple forms, includes: Langerhans cell histiocytosis, other non-Langerhans cell histiocytosis (cephalic histiocytosis, generalized eruptive histiocytoma, giant cell reticulohistiocytoma), urticaria pigmentosa, tuberous xanthomas, dermatofibroma, angiomas, nevus, molluscum contagiosum and pyogenic granuloma 5 .…”