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McCune-Albright syndrome with gigantism and hyperprolactinemia
F Pacini1, G Perri, P Bagnolesi
1Istituto di Metodologia Clinica e Medicina del Lavoro, University of Pisa, Italy.
Abstract:
We describe the case of a 38-year-old man with typical Mc Cune-Albright syndrome and the unusual combination of both growth-hormone and prolactin hypersecretion. The patient was extremely tall, which is unusual in Mc Cune-Albright syndrome, suggesting that he did not have precocious fusion of the epiphysis, a common finding in this syndrome. Unfortunately the patient refused any treatment for his disease. A similar case has been previously described only in a 14-year-old boy.
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