The goals of treatment of patients with Acromegaly are to lower the serum IGF-1 concentration to within the normal range for the patient’s age and gender, control/reduce the pituitary tumor size, and reduce the mass effects/compression of the surrounding structures in the brain, improve symptoms and control or reverse the metabolic complications like diabetes mellitus. Dr Thomas will review all the results of the blood tests and the relevant imaging. She will educate you on the condition, explain all the results of the tests, and formulate an individualized treatment plan for you.
The different modalities of treatment of Cushing disease are:
Surgery
Dr Thomas will refer you to an experienced neurosurgeon for evaluation and surgical management of the pituitary tumor.
Postoperatively, Dr Thomas will monitor your clinical symptoms and arrange for you to have blood tests to monitor the reduction in serum IGF-1, the biochemical parameter used to monitor the resolution and recurrence of the tumor. She will also arrange for you to have additional imaging with an MRI of the pituitary gland approximately 12 weeks post-surgery.
You may need additional surgery if the entire tumor is not removed or if the tumor recurs.
Medications
Oral medications are required when surgery has not normalized the serum IGF-1. The medications include long-acting somatostatin analogs that block the cells producing GH or pegvisomant, a medication that blocks the action of GH.
Radiation therapy
If the tumor is large and is incompletely removed by surgery but is still producing either excess GH or causing pressure on the surrounding structures in the brain, then you may need radiation therapy. Radiation therapy helps with tumor growth control as well as in controlling the production of excess hormones from the pituitary gland.