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Acromegaly with multiple secreting pituitary adenomas
Surgical Neurology
|December 1, 1984
Summary
This case study presents acromegaly caused by two distinct growth hormone-secreting pituitary adenomas. Multiple adenomas were identified via CT scan and confirmed during surgery, highlighting a rare occurrence.
Area of Science:
- Endocrinology
- Neurosurgery
- Oncology
Background:
- Acromegaly is a disorder caused by excess growth hormone (GH) production, typically due to a pituitary adenoma.
- Pituitary adenomas are tumors of the pituitary gland, a small gland at the base of the brain.
Observation:
- This report details a rare case of acromegaly in a patient with two separate GH-secreting pituitary adenomas.
- Initial suspicion of multiplicity arose from computerized tomographic (CT) scan imaging.
Findings:
- Transsphenoidal surgery confirmed the presence of two distinct pituitary adenomas.
- Histopathological examination verified that both adenomas were secreting growth hormone.
Implications:
- The findings suggest that multiple pituitary adenomas, though rare, can occur and lead to conditions like acromegaly.
- This case underscores the importance of thorough diagnostic evaluation, including advanced imaging, for complex pituitary disorders.