Acromegaly

Below you will find more information about Acromegaly from Medigest. If you believe that you are suffering from any of the symptoms of Acromegaly it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Acromegaly and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Acromegaly comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.

Definition

Acromegaly was derived from the Greek word 'akros' meaning 'extremities' or 'extreme' and 'megalos' which means 'large'. This is a syndrome which results as the pituitary gland has an overproduction of hGH or growth hormone following the closure of the epiphyseal plate. There are several disorders that could cause the pituitary gland to come up with this circumstance. Most of these conditions involve a tumor that produces GH which is derived from a distinctive cell type (called somatotrophs) and named pituitary adenoma.

Treatment

The objective of treatments is to reduce the production of GH down to the normal levels. This will relieve the tumor pressure on the brain which will preserve the normal function of the pituitary gland. It is also the aim of the treatment to reverse or lessen the symptoms of the disorder. The three most common treatments are surgery (which is the fastest and most effective treatment that is available); radiation therapy (this is a type of treatment that should go together with surgery and drugs), and also drug therapy (the two known medications include Bromocriptine or Parlodel and Sandostatin.

Symptoms and Signs

The characteristics that are common to acromegaly are serious disfigurement, severe conditions that result into complications and even early death when the condition is left unchecked. The most common age range that is affected by this disorder is the early 20's. The disease is often difficult to diagnose during its early stages and it is often missed for many successive years. The disease only becomes apparent when the external features start to manifest the signs. This disorder is usually linked with gigantism. This is when the patient's feet, hands, nose, ears, and lips become thickened. The internal organs also become swollen (more so with the heart which is weakened and also the kidneys); the vocal cords of the patient become weak and thus the voice deepens; a skull expansion at the fontanelle; the brows protrude which often results into ocular distension; the lower jaw also protrudes which also comes with macroglossia and gapping of the teeth. Complications that can result from this disorder are: acute headache; carpal tunnel syndrome; arthritis; enlargement of the heart; hypertension; failure of the heart; diabetes mellitus; kidney failure; optic chiasm compression which leads to vision loss on the outer fields (generally bitemporal hemianopia); an increased sweating of the palms; and production of sebum on the face (also called seborrhea).

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