Machado M C, Alcantara A E E, Pereira A C L, Cescato V A S, Castro Musolino N R, de Mendonça B B, Bronstein M D, Fragoso M C B V
Neuroendocrine Unit, Division of Endocrinology and Metabolism, University of Sao Paulo Medical School, São Paulo, SP, Brazil.
Laboratory of Cellular and Molecular Endocrinology LIM-25, University of Sao Paulo Medical School, São Paulo, SP, Brazil.
J Endocrinol Invest. 2016 Dec;39(12):1401-1409. doi: 10.1007/s40618-016-0504-y. Epub 2016 Jun 30.
Pituitary macroadenomas (MACs) represent 10-30 % of Cushing's disease (CD) cases. The aim of this study was to report the clinical, laboratorial and imaging features and postsurgical outcomes of microadenoma (MIC) and MAC patients.
Retrospective study with 317 CD patients (median 32 years old, range 9-71 years) admitted between 1990 and 2014, 74 (23.3 %) of whom had MAC.
Hirsutism, plethora facial, muscular weakness and muscular atrophy were more frequent in the MIC patients. Nephrolithiasis, osteopenia, hyperprolactinaemia and galactorrhoea were more prevalent in MAC patients. The morning serum cortisol (Fs), nocturnal salivary cortisol (NSC), nocturnal Fs (Fs 2400 h), low- and high-dose dexamethasone suppression test results and CRH and desmopressin test results were similar between the subgroups. MIC patients showed higher urinary cortisol at 24 h (UC), and MAC patients presented higher ACTH levels but lower Fs/ACTH, Fs 2400 h/ACTH, NSC/ACTH and UC/ACTH ratios. There were negative correlations of tumour size with Fs/ACTH, Fs 2400 h/ACTH, NSC/ACTH and UC/ACTH ratios. Overall, the postsurgical remission and recurrence rates were similar between MIC and MAC. However, patients in remission (MIC + MAC) showed smaller tumour diameters and a lower prevalence of invasion and extension on MRI.
Despite exhibiting higher plasma ACTH levels, CD patients with MAC presented lower cortisol/ACTH ratios than did patients with MIC, with a negative correlation between tumour size and cortisol/ACTH ratios. The overall postsurgical remission and recurrence rates were similar between MIC and MAC patients, with those with larger and/or invasive tumours showing a lower remission rate.
垂体大腺瘤(MAC)占库欣病(CD)病例的10% - 30%。本研究旨在报告微腺瘤(MIC)和MAC患者的临床、实验室及影像学特征以及术后结果。
对1990年至2014年间收治的317例CD患者(中位年龄32岁,范围9 - 71岁)进行回顾性研究,其中74例(23.3%)为MAC。
多毛症、面部潮红、肌肉无力和肌肉萎缩在MIC患者中更为常见。肾结石、骨质减少、高泌乳素血症和溢乳在MAC患者中更为普遍。各亚组间晨血清皮质醇(Fs)、夜间唾液皮质醇(NSC)、夜间Fs(Fs 2400 h)、低剂量和高剂量地塞米松抑制试验结果以及促肾上腺皮质激素释放激素(CRH)和去氨加压素试验结果相似。MIC患者24小时尿皮质醇(UC)较高,MAC患者促肾上腺皮质激素(ACTH)水平较高,但Fs/ACTH、Fs 2400 h/ACTH、NSC/ACTH和UC/ACTH比值较低。肿瘤大小与Fs/ACTH、Fs 2400 h/ACTH、NSC/ACTH和UC/ACTH比值呈负相关。总体而言,MIC和MAC患者术后缓解率和复发率相似。然而,缓解患者(MIC + MAC)的肿瘤直径较小,MRI上侵袭和扩展的发生率较低。
尽管血浆ACTH水平较高,但MAC的CD患者的皮质醇/ACTH比值低于MIC患者,且肿瘤大小与皮质醇/ACTH比值呈负相关。MIC和MAC患者术后总体缓解率和复发率相似,肿瘤较大和/或侵袭性肿瘤患者缓解率较低。