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Article
May 3, 1976

Hyperprolactinemia Associated With Empty Sella Syndrome

Author Affiliations

From the Department of Medicine, The Johns Hopkins University and Hospital, Baltimore, and the Washington (DC) Hospital Center.

JAMA. 1976;235(18):2002-2004. doi:10.1001/jama.1976.03260440054027
Abstract

SINCE the radioimmunoassay of human prolactin became available, hyperprolactinemia has been demonstrated in a number of pathological states.1 An elevated basal prolactin concentration of more than 200 ng/ml is generally regarded as strong evidence in favor of an adenomatous pituitary lesion.2 Our patient had substantial hyperprolactinemia associated with the empty sella syndrome.

Report of a Case  A 37-year-old woman was referred to The Johns Hopkins Hospital in December 1973 because of persistent generalized headaches of five years' duration. Three years prior to admission, she underwent extensive examinations in another hospital. Skull roentgenograms had shown enlargement of the sella turcica, with erosion of the dorsum sellae (Fig 1). A right brachial arteriogram showed no abnormalities. Pneumoencephalography was attempted twice, but no air could be driven into the ventricular system (Fig 2). The patient was obese, normotensive, and without visual field defects. Galactorrhea could not be demonstrated. Serum thyroxine level

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