Acromegaly
Acromegaly is a rare condition caused by excess growth hormone, almost always due to a benign pituitary tumour. Because it develops gradually, often over many years, it is frequently diagnosed late - sometimes by chance when a doctor notices characteristic changes in appearance.
Common symptoms
- gradual enlargement of the hands and feet
- changes in facial features such as an enlarged brow, jaw, or lips
- excessive sweating, joint pain, and headaches
What we offer
- the correct blood test (IGF-1) and confirmatory glucose suppression testing
- referral for pituitary MRI to identify the underlying tumour
- clear explanation of treatment options, from surgery to medication
Confirming acromegaly
Diagnosis is based on clinical features together with IGF-1 testing and, when required, an oral glucose suppression test interpreted in context. Pituitary MRI then helps identify the cause. Assessment also considers blood pressure, diabetes, sleep apnoea, heart health, vision, joint symptoms and colon screening needs.
Treatment and long-term monitoring
Treatment commonly involves specialist pituitary surgery, with medicines or radiotherapy used when needed. Follow-up checks biochemical control, pituitary function, imaging and associated health risks because surveillance may continue even after successful treatment.
UK-wide video consultations
Clinical review and most result discussions can take place securely by video, while blood tests, imaging, sleep studies and other investigations are arranged locally.