Published: 18 Jun 2025

ICD9: 253.0      ICD10: E22.0      ICD11: 5A60.0

The phrase "Brain Tumor, Acromegaly" refers to acromegaly that is caused by a brain tumor, specifically a tumor in the pituitary gland.
Let's break that down:

Acromegaly: A hormonal disorder that develops when the pituitary gland produces too much growth hormone (GH) after the growth plates have closed. This results in enlarged hands and feet, a prominent jaw and forehead, and other changes in facial features.

Pituitary Gland: A small gland located at the base of the brain that is responsible for producing several hormones, including growth hormone (GH).

Brain Tumor: A mass or growth of abnormal cells in the brain. In the context of acromegaly, the most common type is a pituitary adenoma, a non-cancerous tumor that develops in the pituitary gland.

Here's how the connection works:

1. Pituitary Adenoma Forms: A tumor develops in the pituitary gland.
2. Excess GH Production: The tumor disrupts the normal function of the pituitary gland, causing it to overproduce GH.
3. Acromegaly Develops: The excess GH leads to the characteristic symptoms of acromegaly.

In essence, "Brain Tumor, Acromegaly" means the acromegaly is a *secondary* condition caused by a tumor (usually benign) on the pituitary gland.

Key points to remember:

Cause: The most common cause of acromegaly is a pituitary adenoma.
Treatment: Treatment typically involves surgery to remove the tumor, medication to control GH levels, or radiation therapy.
Importance of Diagnosis: Early diagnosis and treatment are crucial to prevent or minimize the long-term health complications associated with acromegaly.

If you suspect you or someone you know may have acromegaly, it is essential to consult with a doctor for diagnosis and treatment.