Both acromegaly and gigantism are clinically caused by abnormal secretion of hGH from pituitary tumors, clinically known as growth hormone pituitary adenomas. When the disease develops in children before the bone scale closes, hGH causes rapid skeletal growth, which manifests as abnormally high height in children compared to their peers, commonly known as gigantism. In adults, the disease is often characterized by abnormal development of the hands and feet, enlarged joints, thickened lips and other special features commonly known as acromegaly. In clinical practice, we often encounter patients with acromegaly, who are often diagnosed by chance by experienced physicians in other departments during the course of medical treatment, and who do not have many symptoms themselves. In human body, abnormal increase of hGH, also commonly known as growth hormone, will cause 3 main pathological changes: 1.Promote skeletal growth, manifested as hypertrophy of the extremities, and patients often complain of larger and larger shoe size within 3-5 years. 2.Promote soft tissue growth, manifested as lip hypertrophy and tongue enlargement. Patients have swollen hands and feet and limited fine movements. In addition, some patients have severe snoring due to tongue hypertrophy and swollen pharyngeal tissues, and some patients will have difficulty in breathing. 3.Promote the growth of internal organs, manifested as enlarged liver, gallbladder and spleen, and enlarged heart, so acromegaly is often combined with certain myocardial ischemia or heart conduction block. Through surgery, if the tumor can be removed completely, it will stop the pathological changes in these 3 areas, especially the latter two, and bring better quality of life for the patient. It has been shown that the level of hGH in the blood of patients with acromegaly is inversely proportional to the life expectancy of the patient, that is, the higher the hGH in the blood, the shorter the life expectancy of the patient. Therefore, for patients with growth hormone tumors such as acromegaly, we recommend: 1. early surgical treatment once diagnosed. 2. 2. Pay attention to snoring and heart conditions during the perioperative period, as poor management of these physical conditions may endanger life, and it is best to go to a provincial mainstream neurosurgery center for treatment if possible. 3. Seek professional treatment team or doctors to strive for surgical cure and avoid residual and recurrence.