Yılmaz, Meltemİşcan, ArifMutlu, Levent2024-10-292024-10-2920242149-3189https://doi.org/10.18621/eurj.1208264https://search.trdizin.gov.tr/tr/yayin/detay/1226179https://hdl.handle.net/20.500.11776/12731Methemoglobinemia is a serious hematological disease characterized by the incapability of sufficient oxygen delivery to tissues and cyanosis when iron within hemoglobin in ferrous form (Fe+2) is oxidized to ferric form (Fe+3). Methemoglobinemia may be congenital or acquired. While prilocaine-induced methemoglobinemia can be seen in newborns and early pediatric ages, it is a rare condition in adults. We aimed to investigate prilocaine-induced adult methemoglobinemia with four cases.en10.18621/eurj.1208264info:eu-repo/semantics/openAccessAdultprilocainemethemoglobinemiacyanosisArticle1022492531226179