Understanding Acromegaly: Symptoms, Diagnosis and Treatments

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Understanding Acromegaly: Symptoms, Diagnosis and Treatments
Acromegaly is most commonly seen in adults who have a pituitary adenoma. This adenoma produces excess amounts of Growth Hormone (GH) which affects cartilaginous tissues such as the joints in hands and jaws, as well as the tissue of the nose, ears and heart. Because this growth is occurring after the epiphyseal plates have closed it creates a disproportionate appearance which is typically the first sign in the patient. There are several immunoradio assays to test for serum levels GH, but there is evidence to suggest that these assays are not accurate enough for diagnosis. The current standard is to diagnose using an oral glucose load, levels of GH and Insulin-like Growth Factor (IGF-1). We also use MRI scans that are focused on the sella turcica to investigate the possibility of the pituitary adenoma. There are several methods of treatment including surgery, radiotherapy, radiosurgery and drug therapies that have continued to develop.
Pathophysiology of Acromegaly
The pituitary gland sits at the base of the skull and controls much of our endocrine secretions through a tightly controlled negative feedback system (Norris, 2007). Normally, growth hormone (GH) secretions act to cause bone and muscle growth (Norris, 2007). As we age there is a decline in the amount of GH our bodies produce and use mostly due to the closure of epiphyseal plates which marks the end of vertical growth (Norris, 2007). GH is also important for muscle cells to be able to take up glucose during normal metabolic processes (Norris, 2007). Insulin plays an important role in this pathway and we often see disruptions in both pathways with acromegaly (Katznelson, 2011).
Acromegaly first begins with an a...

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