We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
A Rare Cause of Acromegaly: Short Review of McCune Albright Syndrome.
- Authors
Aydın, Yusuf; Berker, Dilek; Bulut, Sercan; Tütüncü, Yasemin Ateş; Işık, Serhat; Üstün, İhsan; Delibaşı, Tuncay; Güler, Serdar
- Abstract
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.
- Subjects
ACROMEGALY; BONE diseases; SYNDROMES; FIBROUS dysplasia of bone
- Publication
Turkish Journal of Endocrinology & Metabolism, 2009, Vol 13, Issue 1, p13
- ISSN
1301-2193
- Publication type
Case Study