TRUE HAMARTOMA OF THE HYPOTHALAMUS ASSOCIATED WITH PUBERTAS PRAECOX
TRUE HAMARTOMA OF THE HYPOTHALAMUS ASSOCIATED WITH PUBERTAS PRAECOX
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与早熟相关的真正下丘脑错构瘤
DOI:
10.1097/00005072-195110000-00002
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发表时间:
1951
影响因子:
3.2
通讯作者:
R. Richter
中科院分区:
文献类型:
--
作者:
R. Richter
The regulatory influence of the nervous system upon such elaborate and complex events in the life of the organism as body growth and somatic sexual development remains a source of great interest and wonder. The once widely held opinion that macrogenitosomia praecox was specifically related to disease of the pineal gland, notably to tumors arising from it, has been generally discredited. Almost all neurologists and endocrinologists now agree that the hypothalamus, more especially the tuber cinereum, regulates growth and sexual maturation and that it is disease of this area alone that leads to neurogenic pubertas praecox. It will be understood, of course, that cases associated with gonadal or adrenal tumor are excluded. It is unnecessary to review here the evidence that has led to the abandonment of the pineal gland and the adoption of the hypothalamus as the critical site for premature sexual development and maturation of intracranial origin in man. Recent expositions of the argument may be found in the papers of Heuyer, Lhermitte, De Martel and Vogt (1), Horrax and Bailey (2), and Weinberger and Grant (3).This report concerns the neuropathological findings encountered in a female child, 7 years of age, who presented well marked macrogenitosomia praecox beginning very early in life. The value of the observations lies in the fact that the lesion of the hypothalamus which was present, was small and discretely localized, did not damage the hypothalamus proper, and was not complicated by secondary effects upon other parts of the brain.