Imura H, Matsukura S, Yamamoto H, Hirata Y, Nakai Y
Cancer. 1975 May;35(5):1430-7. doi: 10.1002/1097-0142(197505)35:5<1430::aid-cncr2820350529>3.0.co;2-o.
This report describes the clinical and biochemical features of 30 cases of ectopic ACTH-producing tumors diagnosed by the detection of ACTH in the tumor tissues. Several uncommon tumors, such as tumors of the esophagus, stomach, and larynx, were included in this series. None of the patients with bronchogenic carcinoma showed signs of classical Cushing's syndrome, whereas 7 of the remaining 13 patients with other tumors were Cushingoid in appearance. Adrenocortical hyperfunction was present in 61 percent at the first examination and developed during the course of the disease in 18 percent more. In the remaining patients (21 percent), adrenocortical function remained within normal limits. These results indicate that there exist ectopic ACTH-producing tumors without clinical and biochemical sequelae of excess hormone. In some of the tumor extracts studied, MSH and CRF-like activities and serotonin were detected. This suggests that multiple hormone production is not uncommon in ectopic ACTH-producing tumors.
本报告描述了30例通过检测肿瘤组织中的促肾上腺皮质激素(ACTH)诊断出的异位ACTH分泌肿瘤的临床和生化特征。本系列纳入了几种罕见肿瘤,如食管、胃和喉的肿瘤。支气管癌患者均无典型库欣综合征的体征,而其余13例其他肿瘤患者中有7例有库欣样外观。首次检查时61%的患者存在肾上腺皮质功能亢进,病程中又有18%的患者出现肾上腺皮质功能亢进。其余患者(21%)的肾上腺皮质功能保持在正常范围内。这些结果表明,存在无激素过量临床和生化后遗症的异位ACTH分泌肿瘤。在一些研究的肿瘤提取物中,检测到了促黑素(MSH)和促肾上腺皮质激素释放因子(CRF)样活性以及血清素。这表明多种激素分泌在异位ACTH分泌肿瘤中并不罕见。