Discussion Clinical suspicion for acromegaly is confirmed by elevated IGF-1 and GH levels.
When a GH-secreting pituitary adenoma is resected, immunocytochemistry with GH staining …

The diagnosis of acromegaly is suspected based on the typical clinical presentation and is
subsequently confirmed biochemically by elevated GH and IGF-I concentrations. We report …

Methods: We report the clinical history and the laboratory and imaging results of an
acromegalic woman with no clear evidence of pituitary somatotropinoma or ectopic …

The presence of growth hormone (GH) immunostaining in patients who lack the biochemical
and clinical features of acromegaly has been described. In contrast, there is little information …

Discussion The young age at presentation makes this case atypical for acromegaly. He had
classic symptoms of acromegaly and found to have markedly elevated IGF-1 levels. The …

Introduction: Acromegaly can rarely be caused by an ectopic production of GH or GHRH by
various neoplasms, most commonly neuroendocrine tumors of pancreatic or pulmonary …

Acromegaly is a slowly progressing and rare disease due to excessive growth hormone
(GH) that stems from a pituitary adenoma in most cases. GH is a peptide hormone with …

We report a case of acromegaly with relatively low GH secretion in a patient with GH-
secreting pituitary macroadenoma. The 44-year-old male patient presented with left …

Acromegaly is rarely due to an excess of the GH-releasing hormone (GHRH) and pituitary
hyperplasia on histology should alert to its presence. Clinical Case: A 35-year-old was …

Acromegaly is a clinical syndrome caused by the overproduction of growth hormone (GH)
and also known as a rare disease. Clinical, biochemical, and radiological features are often …