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The syndrome of multiple endocrine neoplasia type IIA in three generations of one family (continued 50­years of observation)

https://doi.org/10.14341/serg2015344-48

Abstract

Syndrome Sipple is the second name of the syndrome of multiple endocrine neoplasia type II (MEN­2A). In 1961 J.H. Sipple described several relatives with medullary thyroid cancer, feohromotsytoma and hyperparathyroidism. The following observation is presented.

About the Authors

Sergey Vladimirovich Sergуikо
http://www.chelsma.ru/education/kafedry/obshhej-khirurgii/zavkafedroj/
South Ural State Medical University
Russian Federation
MD, PhD, Professor


Valeriy Alekseevich Privalov
http://www.chelsma.ru/education/kafedry/obshhej-khirurgii/istorija-kafedry/privalov-valerij-alekseevich/
South Ural State Medical University
Russian Federation
MD, PhD, Professor


References

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2. Brandi ML, Gagel RF, Angeli A. Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab. 2001;86(12):5658-5671. PMID: 11739416.

3. Kloos RT. Medullary thyroid cancer: management guidelines of the American Thyroid Association. Thyroid. 2009;19(6): 565-612. doi: 10.1089/thy.2008.0403. PMID: 19469690.

4. Raue F, Frank-Raue K. Multiple Endocrine Neoplasia Type 2. Update. Horm Res. 2007;68:101-104. doi: 10.1159/000110589. PMID: 18174721.


Review

For citations:


Sergуikо S.V., Privalov V.A. The syndrome of multiple endocrine neoplasia type IIA in three generations of one family (continued 50­years of observation). Endocrine Surgery. 2015;9(3):44-48. (In Russ.) https://doi.org/10.14341/serg2015344-48

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ISSN 2306-3513 (Print)
ISSN 2310-3965 (Online)