报告363例肢端肥大症的治疗结果。
AbstractFrom 1954 to 1989, 363 patients with acromegaly were treated by radiotherapy.
还不知这项观察是否能反映出肢端肥大症的一种更为普遍的骨折风险的增加。
It is unknown whether this observation may reflect a more general increased risk of fractures in acromegaly.
背景：关于肢端肥大症骨质疏松骨折的资料有限，在活动性肢端肥大症的绝经后妇女中，可以观察到放射线检测到的椎骨骨折发生率增加。
CONTEXT: Data on osteoporotic fractures in acromegaly are limited. An increased prevalence of radiological vertebral fractures was already observed in postmenopausal women with active acromegaly.
尽管无法治愈的肢端肥大症能导致各种疾病和早逝，但治疗能降低患并发症的风险并显著改善症状。
Although untreated acromegaly can lead to serious illness and premature death, available treatments can reduce your risk of complications and significantly improve your symptoms.
由于肢端肥大症并不常见，而且生理改变是逐渐发生的，因此不会立刻察觉。
Because acromegaly is uncommon and physical changes occur gradually, it often isn't recognized right away.
那些有肢端肥大症或者巨人症(也称为“巨大症”)的人会长得非常高，这通常是由于他们的脑垂体出了问题，成长激素过多。
People who have acromegaly or gigantism (also called giantism) will grow very tall, usually because of problems with their pituitary glands and an overabundance of.
作者报道一例罕见的肢端肥大症出现单侧寰椎关节肥大，导致脊髓受压和进行性四肢轻瘫。
The authors report an extremely rare case of a patient with acromegaly who had unilateral enlargement of an atlas facet resulting in cord compression and progressive quadriparesis.
作者在8例肢端肥大症体外培养的垂体GH瘤细胞上探讨IGF-1对GH分泌的反馈调节作用。
The feedback regulation of IGF-1 on GH secretion from acromegalic pituitary tumors in cell culture was studied in 8 cases.
本文对106例肢端肥大症放射治疗的疗效进行了分析，对本症的临床症状、体征、内分泌实验室检查等作了治疗前后的对比。
During 1962-1982, 106 cases of acromegaly were treated with radiation therapy. By comparing the clinical symptoms, signs and laboratory data before and after therapy, the results were satisfactory.
目的探讨肢端肥大症性心肌病的神经外科手术治疗和疗效。
Objective To study the surgical treatment of the acromegalic cardiomyopathy.
目的探讨肢端肥大症性心肌病的神经外科手术治疗和疗效。
Objective To study the surgical treatment of the acromegalic cardiomyopathy.
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