Diagnosis of Men-I Syndrome on (68)Ga-DOTANOC PET-CT and Role of Peptide Receptor Radionuclide Therapy With (177)Lu-DOTATATE.

作者信息

Kumar Gupta Santosh, Singla Suhas, Damle Nishikant A, Agarwal Krishankant, Bal Chandersekhar

机构信息

Department of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Int J Endocrinol Metab. 2012 Fall;10(4):629-33. doi: 10.5812/ijem.4313. Epub 2012 Sep 30.

MEN-I is a rare genetic disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary gland, and pancreatic islet cells. We present a case of MEN-I syndrome diagnosed using predominantly nuclear medicine imaging followed by radionuclide therapy, thus emphasizing the role of nuclear imaging in diagnosing and treating MEN-I.