Close

We use cookies to give you the best possible online experience. If you continue, we'll assume you are happy for your web browser to receive all cookies from our website. See our cookie policy for more information on cookies and how to manage them.

Acromegaly

Excessive growth of parts of the body due to overproduction of growth hormone by the pituitary gland

  • May occur at any age
  • Occasionally runs in families
  • Gender and lifestyle are not significant factors

Acromegaly is a rare condition that results from overproduction of growth hormone by the pituitary gland. Over-production of growth hormone causes certain bones, particularly those in the face, hands, and feet, to enlarge. Soft tissues, such as the tongue, also become enlarged. Acromegaly may occur at any age. If excess growth hormone is produced during childhood, the condition causes exaggerated bone growth resulting in excessive height, and is called gigantism (see Growth disorders).

Acromegaly is usually caused by a pituitary tumour. In rare cases, acromegaly occurs as part of multiple endocrine neoplasia, an inherited disorder in which tumours develop in several of the endocrine glands around the body.

What are the symptoms?

If acromegaly develops in adulthood, the resulting physical changes occur almost imperceptibly over a period of years. Sometimes, the condition is detected by comparing old photographs with more recent ones. The following symptoms may become noticeable:

  • Changes in the shape of the face, such as enlargement of the jaw.

  • Enlargement of the hands or feet, resulting in a larger glove or shoe size.

  • Deepening of the voice.

  • Enlargement of the tongue.

  • Tingling in the hands and feet.

  • Excessive sweating.

  • Increased growth of coarse body hair.

A growing pituitary tumour may press on the brain, causing headaches and loss of the normal field of vision (see Visual field defects) in addition to the symptoms of acromegaly. If not treated, acromegaly may cause serious disorders, such as diabetes mellitus and enlargement of the heart (see Dilated cardiomyopathy), which may lead to chronic heart failure.

What might be done?

Your doctor may arrange for you to have several blood tests. If these tests reveal high growth hormone levels, you may also undergo imaging procedures, such as MRI or CT scanning, to look for a pituitary tumour.

Small pituitary tumours can usually be removed completely by surgery. If a tumour is large or cannot be removed entirely, radiotherapy may be necessary to destroy the remaining tumour cells, or drugs may be given to reduce the production of growth hormone (see Pituitary drugs).

Treatment is usually effective and prevents life-threatening complications from developing. Soft tissues will gradually decrease in size. However, changes in the size of bones cannot be reversed.

From the 2010 revision of the Complete Home Medical Guide © Dorling Kindersley Limited.

Back to top

Search the
Medical Encyclopedia

The subjects, conditions and treatments covered in this encyclopaedia are for information only and may not be covered by your insurance product should you make a claim.