Autor: |
Yusuf Aydın, Dilek Berker, Sercan Bulut, Yasemin Ateş Tütüncü, Serhat Işık, İhsan Üstün, Tuncay Delibaşı, Serdar Güler |
Jazyk: |
angličtina |
Rok vydání: |
2009 |
Předmět: |
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Zdroj: |
Turkish Journal of Endocrinology and Metabolism, Vol 13, Iss 1, Pp 13-15 (2009) |
ISSN: |
1301-2193 |
Popis: |
McCune-Albright syndrome (MAS) is characterized by a triad of poly/monostotic fibrous dysplasia, café-au-lait macules, and hyperfunctioning endocrinopathies, including growth hormone (GH) excess. Acromegaly, as a manifestation of endocrine hyperfunction with MAS is uncommon. We report a 34-year-old man with MAS and acromegaly, in whom surgical removal of the pituitary tumour has been technically difficult because of bone deformities. A combination of a long-acting somatostatin analogue (Sandostatin LAR) and external irradiation were therefore used as treatment. Acromegaly associated with MAS is very rarely seen, and has been the subject of approximately 70 published reports. We present a case of acromegaly associated with MAS and a brief survey of relevant literature. Turk Jem 2009; 13: 13-5 |
Databáze: |
OpenAIRE |
Externí odkaz: |
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