Autoimmune Polyglandular Syndrome (Care Report)

N.I. Gurina, P.G. Prudius, M.V. Vlasenko

Abstract


The clinical case reflects polyendocrinopathy of the autoimmune origin that occurs with primary multiple lesions of endocrine glands and other organs. Multiple endocrinopathies mutually aggravate each other and also deteriorate the course of the disease. The basis of pathogenetic treatment is a continuous hormone replacement therapy in functional failure of affected endocrine glands. The early detection of autoimmune polyglandular syndrome and timely treatment help to control the disease.


Keywords


autoimmune polyglandular syndrome type 2

References


Endocrinology. Guidance for physicians. T.2. Diseases of pancreas, parathyroid glands and reproductive system. Ed. SB. Shustov. Sankt-Peterburg, 2011:279-281. (Russian)

Endocrinology. National Guidance. Ed. II.Dedov, GA. Melnichenko. М.: GЕОТАR-Media, 2008:937-943. (Russian)

Larina АА, Тroshina ЕА, Ivanova ОN. Autoimmune polyglandular syndromes of adults: genetic and immunological criteria of diagnostics. Problemy Endocrinologii. 2014;3:43-48. (Russian)

Larina АА, Тroshina ЕА. Latent forms of autoimmune polyglandular syndrome of adults: features of diagnostics and management of patients. Теrapevtycheskiy arkhiv. 2014;10:73-76. (Russian)




DOI: https://doi.org/10.22141/2224-0721.7.79.2016.86420

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