Singer W, Kovacs K, Ryan N, Horvath E
J Clin Pathol. 1978 Jun;31(6):591-8. doi: 10.1136/jcp.31.6.591.
Ten out of 164 cases of bronchogenic carcinoma showed pathological evidence at necropsy of the ectopic ACTH syndrome. All occurred in association with oat-cell carcinoma, constituting 19% of that group. The pathological features consisted of adrenocortical hyperplasia confined to the zona fasciculata and Crooke's hyaline change in the pituitary. Immunoperoxidase stainable ACTH was detected in the pituitary but not in the carcinoma tissue, a surprising finding, which may be due to the different nature of ACTH present in tumour tissue. The ectopic ACTH syndrome was diagnosed ante mortem in only four out of 10 patients on the basis of hypokalaemia and metabolic alkalosis. The lack of clinical pointers in all but terminal cases is discussed as well as possible measures for earlier diagnosis.
164例支气管源性癌患者中,有10例在尸检时显示有异位促肾上腺皮质激素(ACTH)综合征的病理证据。所有病例均与燕麦细胞癌相关,占该组病例的19%。病理特征包括局限于束状带的肾上腺皮质增生以及垂体的克罗克透明变性。垂体中检测到免疫过氧化物酶可染色的ACTH,但癌组织中未检测到,这一发现令人惊讶,可能是由于肿瘤组织中存在的ACTH性质不同。10例患者中只有4例在生前根据低钾血症和代谢性碱中毒诊断出异位ACTH综合征。讨论了除终末期病例外所有病例缺乏临床指征的情况以及早期诊断的可能措施。