肢端肥大症
生长细胞
医学
内科学
内分泌学
病态的
生长激素
胰岛素样生长因子
垂体腺瘤
激素
生长因子
腺瘤
受体
作者
Carolina Peixe,Miriam Sánchez-García,Ashley Grossman,Márta Korbonits,Pedro Marques
标识
DOI:10.1016/j.ghir.2022.101467
摘要
The most frequent diagnosis underlying the finding of an elevated growth hormone (GH) and insulin-like growth factor-1 (IGF-1) is acromegaly due to a GH-secreting pituitary tumour. However, GH and IGF-1 levels can be discordant in patients with acromegaly due to early or partially treated disease, or there might be another cause of high GH or high IGF-1 unrelated to acromegaly, such as pre-analytical and technical pitfalls, physiological circumstances and pathological conditions. High GH and normal or low serum IGF-1, or alternatively, normal GH with elevated serum IGF-1, should be carefully assessed to avoid misinterpreting the activity of acromegaly or misdiagnosing a patient with acromegaly. We summarise here these biochemical discrepancies in the evaluation of the somatotroph axis.
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