Abstract
BABINSKI (i) in 1900 described the case of a girl with obesity and failure to mature sexually. These symptoms were associated with an intracranial expanding lesion in the region of the sella turcica. Frohlich (2) in 1901 described a boy with a similar clinical picture and diagnosed a tumor of the hypophysis. This syndrome of obesity and infantilism has come to be known as Frohlich’s syndrome or adiposogenital dystrophy. The early experimental ablations of the hypophysis carried out by Crowe, Cushing and Homans (3), and by Aschner (4), suggested a hypopituitary origin to this syndrome. However, Camus and Roussy (5) and Bailey and Bremer (6) pointed out that these early operations were invariably accompanied by damage to the hypothalamus. These workers claimed this latter injury was the true cause of the syndrome. The conflict remained unsettled until the fundamental work of P. E. Smith (7). Smith was able to remove the hypophysis without injury to the h y pothalamus and conversely, to produce a lesion in t...
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: The Journal of Clinical Endocrinology & Metabolism
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.