| Literature DB >> 3680873 |
F Pacini1, G Perri, P Bagnolesi, A Cilotti, A Pinchera.
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.Entities:
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Year: 1987 PMID: 3680873 DOI: 10.1007/BF03348161
Source DB: PubMed Journal: J Endocrinol Invest ISSN: 0391-4097 Impact factor: 4.256