Research Institute for Nuclear Medicine, Tehran University of Medical Sciences, Tehran, Iran
Abstract
A 29- year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. On physical examination café au lait macular spots were noted on her neck, buttocks and left leg. Bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. Considering the presence of polyostotic fibrous dysplasia, precocious puberty and café au lait macular spots, MacCune-Albright syndrome was confirmed in this patient.
Haghighatafshar, M., Fard-Esfahani, A., Karami, F., Saghari, M., Fallahi, B., Beiki, D., Aghahosseini, F., & Eftekhari, M. (2010). McCune-Albright syndrome: Report of a case. Iranian Journal of Nuclear Medicine, 18(1), 57-61.
MLA
Mahdi Haghighatafshar; Armaghan Fard-Esfahani; Fatemeh Karami; Mohsen Saghari; Babak Fallahi; Davood Beiki; Farahnaz Aghahosseini; Mohammad Eftekhari. "McCune-Albright syndrome: Report of a case". Iranian Journal of Nuclear Medicine, 18, 1, 2010, 57-61.
HARVARD
Haghighatafshar, M., Fard-Esfahani, A., Karami, F., Saghari, M., Fallahi, B., Beiki, D., Aghahosseini, F., Eftekhari, M. (2010). 'McCune-Albright syndrome: Report of a case', Iranian Journal of Nuclear Medicine, 18(1), pp. 57-61.
VANCOUVER
Haghighatafshar, M., Fard-Esfahani, A., Karami, F., Saghari, M., Fallahi, B., Beiki, D., Aghahosseini, F., Eftekhari, M. McCune-Albright syndrome: Report of a case. Iranian Journal of Nuclear Medicine, 2010; 18(1): 57-61.
)