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Article
February 1933

SIMMONDS' DISEASE (CACHEXIA HYPOPHYSEOPRIVA): REPORT OF A CASE WITH POSTMORTEM OBSERVATIONS AND A REVIEW OF THE LITERATURE

Author Affiliations

NEW YORK

From the Medical Service, Mount Sinai Hospital.

Arch Intern Med (Chic). 1933;51(2):175-199. doi:10.1001/archinte.1933.00150210005002
Abstract

Simmonds' disease may be defined as a clinical state, most common in women, characterized by progressive, extreme emaciation, premature aging, wrinkling of the facial skin, loss of pubic and axillary hair, dental caries and loss of libido and sexual function, accompanied by a depression of the basal metabolic rate. Untreated, it is a progressively fatal disease, usually terminating suddenly with a short period of coma. There are often mental disturbances closely simulating Korsakoff's syndrome, so that the patients are sometimes first seen by the psychiatrist. The pathologic basis for the condition is varied. In general, it may be said that any process that destroys the anterior lobe of the pituitary gland may give rise to the clinical picture. A "splanchnomicria," an abnormal smallness of the viscera, is the only constant postmortem observation aside from changes in the pituitary body. This was first pointed out by Simmonds.1

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