diagnosis of men-i syndrome on 68ga-dotanoc pet-ct and role of peptide receptor radionuclide therapy with 177lu-dotatate

نویسندگان

santosh kumar gupta department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]; department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]

suhas singla department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]

nishikant a damle department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]

krishankant agarwal department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]

چکیده

abstract 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.

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منابع مشابه

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

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.

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عنوان ژورنال:
international journal of endocrinology and metabolism

جلد ۱۰، شماره ۴، صفحات ۶۲۹-۶۳۳

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