You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


Advertisement

ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | RSS | Access Rights | Sign In


  Vol. 140 No. 4, April 1980 TABLE OF CONTENTS
  Online Only
 •  Online First Table of
Contents
  CLINICAL OBSERVATIONS
 •Online Features
 This Article
 •References
 •Full text PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (15)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Delicious Add to Digg Add to Facebook Add to Reddit Add to Technorati Add to Twitter What's this?

Hypoglycemia in Pregnancy

Occurrence due to Adrenocorticotropic Hormone and Growth Hormone Deficiency

LTC Robert C. Smallridge, MC; Dominic F. Corrigan, MD; LTC Albert M. Thomason, MC; MAJ Peter W. Blue, MC

Arch Intern Med. 1980;140(4):564-565.


Abstract



• Severe symptomatic hypoglycemia (serum glucose level, 24 mg/dL) developed in a 23-year-old, 147.3-cm-tall woman during her late second and early third trimesters of pregnancy. Endocrine studies disclosed insulin levels < 2 µU/mL; growth hormone level < 3 ng/mL; and cortisol level < 1 µg/dL. Hydrocortisone therapy corrected her hypoglycemia, and she was delivered of a healthy female infant. Postpartum, her evaluation included normal thyroid function studies, a normal thyroidstimulating hormone response to protirelin (thyrotropin-releasing hormone), normal serum and urine gonadotropin levels, normal serum prolactin, normal sella turcica tomograms, and a normal EMI brain scan. Urine 17-hydroxycorticosteroids increased during a four-day cosyntropin infusion, but failed to rise after metyrapone administration. The growth hormone level failed to rise after stimulation with levodopa and propranolol administration. The patient was believed to have idiopathic partial hypopituitarism, with hypoglycemia being due to adrenocorticotropic hormone (ACTH) and growth hormone deficiency and the drain of maternal glucose by the fetus. It is suggested that pregnant women with symptomatic hypoglycemia be treated with glucocorticoids while awaiting the results of their endocrine evaluation.

(Arch Intern Med 140:564-565, 1980)



Author Affiliations



USA; USA; USA

From the Division of Endocrinology and Clinical Investigation Service (Drs Smallridge and Corrigan), the Division of Nuclear Medicine (Dr Blue), Walter Reed Army Medical Center, Washington, DC, and Brooke Army Medical Center, San Antonio, Tex (Dr Thomason).


Footnotes



Accepted for publication Aug 20, 1979.

The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or reflecting the views of the Department of the Army or the Department of Defense.

Reprint requests to Division of Endocrinology-Metabolism, Walter Reed Army Medical Center, Washington, DC 20012 (Dr Smallridge).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Delicious Delicious   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Lymphocytic Hypophysitis with Isolated Corticotropin Deficiency
JENSEN et al.
ANN INTERN MED 1986;105:200-203.
ABSTRACT  

Spontaneous Hypoglycemic Seizures in Pregnancy: A Manifestation of Panhypopituitarism
Notterman et al.
Arch Intern Med 1984;144:189-191.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | PHYSICIAN JOBS | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1980 American Medical Association. All Rights Reserved.