Department of Neurosurgery, Emory University School of Medicine, Atlanta, GA, United States.
Department of Neurosurgery, Mayo Clinic, Rochester, MN, United States.
Front Endocrinol (Lausanne). 2022 Aug 4;13:924589. doi: 10.3389/fendo.2022.924589. eCollection 2022.
Acromegaly is a disease that occurs secondary to high levels of GH, most often from a hormone-secreting pituitary adenoma, with multisystem adverse effects. Diagnosis includes serum GH and IGF-1 levels, and obtaining an MRI pituitary protocol to assess for a functional pituitary adenoma. Attempted gross total resection of the GH-secreting adenoma is the gold standard in treatment for patients with acromegaly for a goal of biochemical remission. Medical and radiation therapies are available when patients do not achieve biochemical cure after surgical therapy.
肢端肥大症是一种由 GH 水平升高引起的疾病,最常见于由分泌激素的垂体腺瘤引起,伴有多系统不良影响。诊断包括血清 GH 和 IGF-1 水平,并进行垂体 MRI 方案以评估功能性垂体腺瘤。对于肢端肥大症患者,试图进行 GH 分泌腺瘤的大体全切除是治疗的金标准,目的是实现生化缓解。当患者在手术治疗后未达到生化治愈时,可采用药物和放射治疗。