Dikici, BünyaminUzun, HakanÇapan, KoncaKocamaz, HalilYel, Servet2020-04-302020-04-3020081896-1126https://doi.org/10.2478/v10039-008-0013-0https://hdl.handle.net/20.500.12684/2293dikici, bunyamin/0000-0001-7572-6525WOS: 000207602800035PubMed: 18614441Gianotti-Crosti syndrome (papular acrodermatitis of childhood), which was first described in 1955, is a nonspecific rash that usually consists of the abrupt onset of pink flesh coloring, smooth or lichenoid, flat-topped papules. It was first related to hepatitis B virus (HBV) infection; however, cases not associated with HBV infection were reported as well. Although a type of delayed hypersensitivity reaction is speculated as a cause, exact pathogenesis still remains unclear. The prognosis is favorable and successful management relies upon general supportive and symptomatic care. We report a seven-year-old boy diagnosed with Gianotti-Crosti syndrome with monomorphous papules on his cheeks, buttocks and extremities associated with hepatitis B virus infection.en10.2478/v10039-008-0013-0info:eu-repo/semantics/closedAccessGianotti-Crosti syndromeHepatitis B infectionArticle532338340Q2N/A