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Iukina M.Iu.
FGU Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Goncharov N.P.
FGU Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Bel'tsevich D.G.
Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Troshina E.A.
Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Multiple type 2 endocrine neoplasia (case report)
Journal: Problems of Endocrinology. 2011;57(6): 21‑26
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To cite this article:
Iukina MIu, Goncharov NP, Bel'tsevich DG, Troshina EA. Multiple type 2 endocrine neoplasia (case report). Problems of Endocrinology. 2011;57(6):21‑26. (In Russ.)
The congenital form of pheochromocytoma is known to be fraught with high risk of post-treatment relapse, bilateral, multicentric or primarily multiple lesions. The patients presenting with the syndrome of multiple type 2 endocrine neoplasia usually have no extra-adrenal pheochromocytomas or metastases. Both examination and treatment of these patients should be performed taking these peculiarities into consideration. We describe a family with multiple type 2 endocrine neoplasia and highlight selected aspects of the management of the patients presenting with genetically determined pheochromocytoma.
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Iukina M.Iu.
FGU Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Goncharov N.P.
FGU Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Bel'tsevich D.G.
Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
Troshina E.A.
Éndokrinologicheskiĭ nauchnyĭ tsentr, Moskva
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