Multiple endocrinal neoplasia, 2 В type. Clinical cases
Z.A. AFANASIEVA1,2, A.V. GALEEVA3, М.R. SHAIDULLINA3,4, G.Sh. IMINOV1,2
1Kazan State Medical Academy — Branch Campus of RMACPE MH Russia, Kazan
2Tatarstan Cancer Center, Kazan
3Children’s Republic Clinical Hospital of the MH of RT, Kazan
4Kazan State Medical University, Kazan
Contact:
Afanasieva Z.A. ―MD, Professor of the Oncology, Radiology and Palliative Medicine Department, Head of the Center for the diagnosis and treatment of patients with thyroid and other endocrine organs tumors
Address: 36 Butlerov Str., Kazan, Russian Federation, 420012, e-mail: z-afanasieva@mail.ru
Objective ― to systematize the modern data on multiple endocrine neoplasia syndrome, type 2B (MEN 2B).
Conclusion. The presented clinical observations demonstrate that children’s endocrinologists, pediatricians, and endocrinologist must be wary about MEN 2B syndrome. It may facilitate early diagnostics, timely treatment and improve prognosis in general.
Key words: multiple endocrine neoplasia syndrome (MEN), type 2B, thyroid medullar cancer, pheochromocytoma.
(For citation: Afanasieva Z.A., Galeeva A.V., Shaidullina М.R., Iminov G.Sh. Multiple endocrinal neoplasia, 2 В type. Clinical cases. Practical medicine. 2019. Vol. 17, № 5, P. 169-172)
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