The tumor secretes excessive amounts of growth hormone causing many of the signs and symptoms of acromegaly.
Acromegaly is a syndrome that results when the pituitary gland produces excess growth hormone after epiphyseal plate closure. The name “acromegaly” comes from the Greek words for “extremities” and “great”, because one of the most common symptoms of this condition is abnormal growth of the hands and feet. There are no known risk factors for acromegaly other than a prior history of a pituitary tumor. Acromegaly usually affects middle-aged adults. In children who are still growing, too much growth hormone can cause a condition called gigantism. These children have exaggerated bone growth and an abnormal increase in height. Most cases of acromegaly are caused by a noncancerous tumor (adenoma) of the pituitary gland.
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Autoimmune hepatitis can produce after such viral infections as intense hepatitis A, hepatitis B or measles or after transmission with the Epstein-Barr virus.
Autoimmune hepatitis is a disease in which the system’s exempt structure attacks liver cells. Although the cause for this isn’t completely clear-cut, some diseases, toxins and drugs may spark autoimmune hepatitis in vulnerable folk, particularly women. The disease is normally rather severe and, if not treated, gets worse over moment. Usually, the exempt structure does not respond against the system’s own cells. However, sometimes it erroneously attacks the cells it is supposed to defend. This reaction is called autoimmunity. Some medications wound the liver immediately - overdoses of the popular pain backup acetaminophen, for instance, can induce liver bankruptcy. Other hereditary abnormalities may have autoimmune hepatitis more competitive and harder to handle.
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