Corticotrophin, growth hormone and prolactin deficiencies with hypoaldosteronism and corticosteroid-reversible hypothyroidism in Sheehan's syndrome. Clinical and anatomical correlations

R. M. Jordan, D. M. Cook, W. J. McDonald, D. C. Houghton, J. W. Kendall

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

Deficiencis of corticotrophin (ACTH), growth hormone, and prolactin were documented in a woman with diabetes mellitus and Sheehan's syndrome. The patient's ACTH deficit appeared to be secondary to a hypothalamic abnormality since on two occasions the patient had a marked plasma ACTH response to vasopressin but not to insulin induced hypoglycaemia. It is postulated that the deficits of these three adenohypophysial hormones were instrumental in causing a severely impaired aldosterone secretory capacity in response to sodium restriction and an angiotensin infusion. In addition, the patient had an unusual form of thyroid dysfunction that was in part reversed with hydrocortisone replacement. The patient's unfortunate death during a hypoglycaemia crisis allowed correlation between her extensive antemortum endocrine testing and her pathologic anatomy.

Original languageEnglish (US)
Pages (from-to)12-22
Number of pages11
JournalUnknown Journal
Volume95
Issue number1
DOIs
StatePublished - 1980

ASJC Scopus subject areas

  • Endocrinology

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