Symptoms Checker8
Our recorded sessions provide valuable insights from leading healthcare professionals, researchers, and individuals who are living with Acromegaly and Cushing's Disease.
Increase in shoe size
Increase in the size of hands
(Example: patient needed to buy bigger gloves or noticed an increase in ring size and others)
Any abnormal facial features (compared to old photographs)
(Example: swollen lips and tongue, enlarged nose, protruding forehead, protruding lower jaw and others)
History of or existing Cardiac disease (including biventricular hypertrophy and diastolic or systolic dysfunction)
Carpel tunnel syndrome
Colonic polyps
Diaphoresis (excess perspiration or oily sweating)
Diffuse arthralgia (large joint pains)
Fatigue
Persistent headache
Visual field defects
New-onset or uncontrolled diabetes
New-onset or difficult-to-control hypertension
Amenorrhea
Misalignment of teeth/bite or progressive teeth spacing
Sleep apnoea syndrome (excessive snoring)
Multiple skin tags
You appear to be in good health! Your responses do not currently indicate major symptoms.
Continue to monitor your condition and maintain healthy habits. If new symptoms develop, please reassess or consult a healthcare professional.
Based on your responses, you are showing significant symptoms.
Please visit your nearest Klinik Kesihatan or healthcare provider for further diagnosis and medical advice as soon as possible.
UNDERSTANDING DISEASE
Acromegaly is a rare endocrine disorder that results from an overproduction of growth hormone, typically caused by non-cancerous pea-sized gland named pituitary gland. The overproduction of growth hormone has resulted to abnormal growth of bones and tissues resulted in enlarged hands, feet, facial features and chronic metabolic disorders e.g. hypertension, hypercholesterolemia and diabetes.


Prevalence of Acromegaly


Prevalence Mean age of diagnosis 40-50 years old2-4

Affects men and women equally2-3

MORE THAN 95% are due to growth hormone secreting pituitary tumours 5
In rare occasion, non-pituitary neuroendocrine tumours that cause ectopic secretion of growth hormone releasing hormone (GHRH) which may be bronchial, pancreatic, gastrointestinal, thymic and tumours associated with Multiple endocrine neoplasia type 1 (MEN1).


Did you know?
The word acromegaly comes from the Greek words “acro,” meaning extremities, and “megaly,” meaning enlargement.
Symptoms often develop slowly and may be missed. Watch for:

The most common symptom of acromegaly is abnormal growth of the hands and feet.7 With swelling of the hands and feet being an early symptom of the condition, people with acromegaly might notice that their rings or shoes have become too tight. Over time, as the bones continue to grow, facial features begin to change.
With the brow and lower jaw becoming more prominent, the bone of the nose becoming larger, and the teeth developing spaces between them. Acromegaly can also lead to arthritis, carpal tunnel syndrome, and enlargement of the internal organs, including the heart.7

Additional symptoms may include:
If left untreated, acromegaly can lead to serious complications like:
High Blood Pressure

22.3% – 76.8%9
Type 2 Diabetes

18% –77%9
High Cholesterol

up to 61%9
Overweight

>40%9

Did you know?
Early treatment may help to control symptoms, prevent or manage complications like heart disease and diabetes, and improve quality of life.
COMPLICATIONS
Cardiovascular
You may develop arterial hypertension and or cardiomyopathy (increased size and volume of the heart) with abnormalities in cardiac contractility, sometimes severe heart valve pathologies, or heart rhythm or conduction disorders. Certain cardiac signs may be a result of arterial hyper-tension. GH acts on the muscle of the heart (myocardium), causing hypertrophy (increase in size) of muscle fibres and collagen tissue, thus increasing the size of the heart9
Respiratory
You may suffer from sleep apnoea, and snoring. 2,15,16
Metabolic
GH increases blood glucose levels and exerts a lipolytic effect, which can lead to diabetes and disrupt the balance of fatty acids. 2,17,18
Gastrointestinal tumours
The incidence of polyps in the colon may be higher in patients with acromegaly. 2.15
Endocrine
Excess GH can cause disorders in thyroid function, the development of multinodular thyroid goitres and and hyperparathyroidism. The risk of cancer may be increased ac-cording to certain studies. 2.19
Skeletal and rheumatological
You may suffer from osteoporosis, vertebral fractures, and painful bone and joint pathologies, which can reduce joint mobility and progress to true osteoarthritis. 2.15
Neurological
Carpal tunnel syndrome, most of-ten nocturnal paraesthesia ("tin-gling") can occur in the hands as a result of damage to the median nerve (in the palm of the hand). 2,16

The goal is to bring hormone levels (e.g. IGF-1 and GH) back to normal level and relieve of symptoms.
Treatment options may include:
LEARN MORE
Surgery – 1st line treatment option
Surgical removal of the adenoma is the treatment of choice for patients with acromegaly.1,2 Surgery can provide immediate control of GH levels in the blood, improve symptoms and reduce adenoma volume.
In some cases, patients may require medical therapy before surgery. Surgery results in remission rates of 66–90% for patients with microadenomas, >70% for patients with macroadenomas confined to the sella turcica, 40–50% for patients with non invasive macroadenomas, and <20% for patients with invasive macroadenomas.3,4 The results are better when the adenoma is small and minimally invasive, and when pre-operative GH levels are low.5
Today, the surgery is usually done using often endoscopic microsurgical techniques, passing through the nostril, following the nasal septum and then the sinuses to reach the sphenoid sinus and, eventually the pituitary gland (this is the transsphenoidal route).4
Surgery may be contraindicated or inappropriate, for example if the adenoma is invasive. Medical treatment can then be offered as first line treatment.2
Medical Therapy – 2nd line option
If surgical treatment does not lead to remission or is not an option, medical treatment is often the second approach recommended.1
Medical treatments currently comprise the following types:1
1. Somatostatin receptor ligands (reduce the amount of GH produced).
2. GH receptor antagonists (block the action of GH on GH receptors).
3. Dopamine receptor agonists (reduce the amount of GH produced).
Radiation therapy
The doctor may also suggest revision surgery or radiation therapy (conventional or stereotactic by gamma knife), depending on the size and location of the adenoma and the residual amount of hormones.2
The goal is to bring hormone levels back to normal and relieve symptoms.
If you've experienced unusual changes in your body or health, don’t ignore them.
Talk to your doctor. Early diagnosis can make a big difference.

Can affect many parts of your body. The manifestations and their intensity can vary.
These includes:
WHAT YOU CAN DO
Know what to do before your visit
When you make the appointment, ask if there's anything you need to do to prepare for testing.
Write down any symptoms you're having
Include any that seem unrelated to the appointment. For example, if you've had headaches more often or if you've been feeling down or more tired than usual, tell your health care provider. Also talk to your provider about changes in your appearance, such as weight gain, new acne or more body hair.
Write down key personal information
Let your provider know if the people closest to you have noticed that you seem irritable or have more mood swings than in the past. It may help to bring a photo of yourself that shows any changes in your appearance since you've started having symptoms.
Make a list of all medicines, vitamins, creams or supplements
Write down the name, dose and dates of any steroid medicines you've taken before, such as cortisone shots.
Take a family member or friend along, if possible
Sometimes it can be hard to remember all the information you get during an appointment. Someone who comes with you may remember something that you missed or forgot.
Write down questions
To ask your health care provider
References
Let’s get started. Please let us know whether you are a patient seeking support or a licensed healthcare professional.
We value your privacy
To offer you a better browsing experience, we use cookies to analyze site performance, personalize content, and enable certain features. By continuing, you agree to the use of cookies as described in our Cookie Policy.
Disclaimer
This site contains medical information that is intended for Healthcare Professionals only and is not meant to substitute for the advice provided by a medical professional.
All decisions regarding patient care should be made considering the unique characteristics of the patient.
Viewing As