Endocrinology Research and Practice
Case Report

Acromegaly with No Evidence of Pituitary Adenoma or Ectopic Source

1.

Kırıkkale University Faculty of Medicine, Department of Endocrinology and metabolism, Kırıkkale, Turkey

Endocrinol Res Pract 2017; 21: 92-95
DOI: 10.25179/tjem.2017-56489
Read: 1838 Downloads: 572 Published: 01 September 2017

ABSTRACT

Acromegaly is caused by the uncontrolled hypersecretion of growth hormone (GH) and secondary increases of insulin-like growth factor–1. More than 95% of patients with acromegaly have a growth hormone-secreting pituitary adenoma. Ectopic GH or growth hormone releasing hormone (GHRH)-secreting tumors are rare cause of acromegaly. Pituitary adenomas that cause the hypersecretion of GH are nearly always visible on magnetic resonance imaging. Rarely, patients without an ectopic source may have normal pituitary imaging. In managing this rare circumstance, exploring pituitary or medical treatment with a somatostatin analog might be useful. We describe a patient with acromegaly with no pituitary adenoma and no evidence of ectopic source, who was treated with long-acting octreotide.

 

 

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