Bodakçi, ErdalTuna, Mazhar MüslümKılınç, FarukPekkolay, ZaferSoylu, HikmetTuzcu, Şadiye AltunTuzcu, Alpaslan Kemal2020-03-292020-03-292015Bodakçi, E., Tuna, M.M., Kılınç, F., Pekkolay, Z., Soylu, H., Tuzcu, Ş.A. ve diğerleri. (2015). A rare cause of acromegaly: McCune-Albright syndrome. Dicle Tıp Dergisi, 42(2), 242-244.1300-29451308-9889https://hdl.handle.net/11468/5063http://www.diclemedj.org/upload/sayi/36/Dicle%20Med%20J-02416.pdfhttps://app.trdizin.gov.tr/publication/paper/detail/TVRneE5EZzVPUT09https://search.trdizin.gov.tr/yayin/detay/181489McCune-Albright syndrome is characterized by polyostatic fibrous dysplasia, brown spots on the skin (café au lait pigmentation) and autonomous endocrine hyperfunction. Early puberty and other endocrinological manifestations, such as acromegaly, gigantism and hypercortisolism are widely observed in the syndrome. Acromegaly is seen in 20% of patients. We report a case of acromegaly accompanied with this syndromeMcCune-Albright sendromu, poliostotik fibröz displazi, deride kahverenginde lekelenme (Cafe au lait lekeleri) ve otonomik endokrin hiperfonksiyon ile karakterize bir sendromdur. Bu sendromda yaygın olarak erken puberte ve diğer endokrinolojik manifestasyonlar örneğin akromegali, jigantizm, hiperkortizolizm görülebilir. Akromegali Mc-Cune-Albriht sendromlu hastaların % 20 sinde görülebilir. Biz bu sendroma eşlik eden bir akromegali vakasını sunduk.enAttribution-NonCommercial 3.0 United Statesinfo:eu-repo/semantics/closedAccessMcCune-Albright syndromeAcromegalyFibrous dysplasiaMcCune-Albright sendromuFibröz displaziAkromegaliArticle42224224418148910.5798/diclemedj.0921.2015.02.0564