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May 1986

Transient Elevation of Serum Growth Hormone Level During Pituitary Apoplexy in Acromegaly

Author Affiliations

From the Department of Internal Medicine, Keio University School of Medicine, Tokyo. Dr Taniyama is now at the Veterans Administration Medical Center, Dallas.

Arch Intern Med. 1986;146(5):1001-1003. doi:10.1001/archinte.1986.00360170259033

• We report a case of acromegaly followed by pituitary apoplexy in which hormonal changes during the course of an acute episode were investigated. Serum growth hormone level increased markedly during the acute phase, and, subsequently, decreased rapidly. Finally, serum growth hormone level remained low and did not respond to stimulation. In contrast, the serum cortisol level remarkably decreased during the most serious stage and returned to the previous level after pituitary apoplexy. The low level of cortisol during the acute phase is compatible with the patient's manifestation of adrenal insufficiency, and hydrocortisone sodium succinate administration improved the critical state of the patient dramatically.

(Arch Intern Med 1986;146:1001-1003)