Koca, RafetBektaş, SibelAltınyazar, Hilmi CevdetSezer, Tuna2020-03-262020-03-2620111013-90872005-3894https://dx.doi.org/10.5021/ad.2011.23.4.508https://hdl.handle.net/20.500.12395/26188Histiocytic skin disorders are usually classified as either Langerhans' cell histiocytosis (LCH) or non LCH, based on the pathology. Benign cephalic histiocytosis (BCH) is a rare type of non-Langerhans histiocytitic disorder and is characterized by self-healing multiple small eruptions of yellow to red-brown papules on the face and upper trunk. Histologic features of this disorder show dermal proliferation of histiocytes that have intracytoplasmic comma-shaped bodies, coated vesicles and desmosome-like structures. In this study, we report on a 7-month-old boy who contained small yellow-red papules on his face that spread to his upper trunk. The clinical and histologic features in this patient were consistent with BCH. (Ann Dermatol 23(4) 508 similar to 511, 2011)en10.5021/ad.2011.23.4.508info:eu-repo/semantics/openAccessBenign cephalic histiocytosisGeneralized eruptive histiocytomaInfantjuvenile xanthogranulomaNon-Langerhans-CellArticle23450851122148022Q3WOS:000296942200016Q4