Volume 27, Issue 4 pp. 385-390

Hyperprolactinaemia in males

A heterogeneous disorder

J. P. Walsh

Corresponding Author

J. P. Walsh

NHMRC Postgraduate Medical Scholar, Prince Henry's Institute of Medical Research, Melbourne, Vic

*Registrar, Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, WA.

Prince Henry's Institute of Medical Research, P.O. Box 5152, Clayton, Vic 3168Search for more papers by this author
P. T. Pullan

P. T. Pullan

Clinical Associate Professor, Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, WA

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First published: 25 March 2008
Citations: 36

Abstract

Background: The literature suggests that men with prolactinomas typically present with pressure effects of large pituitary tumours and/or the clinical features of hypogonadism. A definitive study of the clinical features of hyperprolactinaemia in males is, however, lacking.

Aims: To identify the clinical, biochemical and radiological features of hyperprolactinaemia in males.

Methods: Retrospective review of tlie case notes of 53 adult males with prolactinoma or idiopathic hyperprolactinaemia diagnosed 1980–1995.

Results: The mean age of the patients was 41 years (range 19–75). The presenting symptom was endocrine in nature in 57% of patients (loss of libido/potency 47%, gynaecomastia 6%, galactorrhoea 2%, sparse beard growth 2%), pressure effects of pituitary tumour in 28% (headache 13%, visual loss 13%, diplopia 2%), while 15% of patients presented incidentally. On physical examination, galactorrhoea was present in 8% of patients, gynaecomastia in 23

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