A difficult endocrinological patient in oncological practice. Own clinical obseration

Abstract

Klinefelter syndrome is a genetic disease in males (1 per 1000 newborns) due to the presence of a doubled X chromosome in the karyotype (47XXY karyotype), the most common cause of primary hypogonadism. It is characterized by polymorphism of clinical manifestations, the most common of which are primary male infertility, obesity, metabolic syndrome, type 2 diabetes mellitus, osteopenia and osteoporosis. Clinical variability leads to the development of associated conditions against the background of changes in hormonal regulation and observation by different specialists, as a result to late diagnosis of the syndrome. Endogenous hypercorticism in 2030 % is caused by Itsenko Cushing's syndrome, in the structure of which about 7080 % are unilateral adrenal adenomas (corticosteromas). ACTH-independent hypercorticism leads to a number of metabolic and cardiovascular disorders, including abdominal obesity, arterial hypertension, steroid diabetes, and osteoporosis. Long-term suppression of ACTH, according to the feedback principle, leads to suppression of the secretion of hormones of the pituitary endocrine glands (including sex steroids). The clinical observation illustrates the complex pathophysiological disorders that occur when the hypothalamic-pituitary-adrenal / gonadal axis is disturbed in a combination of two syndromes, as well as the importance of a comprehensive examination of endocrinological patients.